From Surf Wiki (app.surf) — the open knowledge base
Haplogroup F (mtDNA)
Human mitochondrial DNA haplogroup
Human mitochondrial DNA haplogroup
| Field | Value |
|---|---|
| name | F |
| map | Peopling of eurasia.jpg |
| origin-date | 43,400 YBP |
| origin-place | Asia |
| ancestor | R9 |
| descendants | F1, F2, F3, F4 |
| mutations | 249d, 6392, 10310 |
the human mtDNA haplogroup
|origin-date=43,400 YBP |origin-place = Asia
Haplogroup F is a human mitochondrial DNA (mtDNA) haplogroup. The clade is most common in East Asia and Southeast Asia. It has not been found among Native Americans.
It is a primary branch of haplogroup R9.
Distribution
The F haplogroup is fairly common in East Asia. High frequencies of the clade are found among the Lahu from Yunnan (33% - 77%, average 52%), Nicobar Islands (50%), Shors from Kemerovo Oblast of Siberia (41%), and Arunachal Pradesh, India (31%). There is also an important frequency in Taiwanese aborigines, Khakas, Kets, Han Chinese (and, thus, nearly all of China), Lombok, Sumba, Thailand, and Vietnam. Its distribution extends with low frequency to the Tharu of southern Nepal and the Bashkirs of the southern Urals.
Haplogroup F also occurs at low frequencies on the Comoros Islands ( It is also found at low frequencies on the Hvar island in Croatia (8.3%).
Subclades
F1a clearly predominates among the representatives of haplogroup F in Southeast Asia, but subclades of this haplogroup have been found in populations as far north as the Buryats and Ulchi of Siberia.
F1b tends to become more frequent as a fraction of total F in populations of the northern parts of East Asia and Central Asia, such as Mongols, Kazakhs, Uyghurs, and Japanese. It also has been found among the Yi people. There are odd exclaves of F1b in Gaininsk Bashkirs of Perm Oblast and Croats of Hvar Island.
F1d is the second most frequent sub-clade in Newar (Nepal). Haplogroup F1d reaches the greatest proportion in Newar (11.97%) of Nepal and Kshatriya (16%) of North India.
F2 has been found mainly in the form of F2a, which has been observed in more than 10% of a couple samples of Nu and Lisu from Gongshan, Yunnan. F2 has been found with frequencies exceeding 5% in several other populations of Southwest China, Guangxi, and Hainan, including the Han majority population. Outside of southwestern China, F2 has been found with frequency greater than 5% in a sample of Oirat Mongols from Xinjiang and a sample of Khakas from Khakassia, with the former population boasting particularly high diversity within this clade.
F3 is especially common among Austronesian peoples of Taiwan and the Malay Archipelago, but it also has been found in many populations of Southwest China and South-Central China, and in a sample of Hans from Xinjiang.
F4 has been found mainly in aboriginal populations of Taiwan and Hainan, with some representatives among samples of Filipinos from Luzon, Indonesians from Sumatra, and Hans and Uzbeks from Xinjiang.
Tree
This phylogenetic tree of haplogroup F subclades is based on the paper by Mannis van Oven and Manfred Kayser Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation and subsequent published research.
- F
- F* – China, Korea
- F1
- F1a'c'f – Thailand (Kaleun in Nakhon Phanom Province), China, Korea, Kazakhstan
- F1a – China, Korea, Uyghur, Thailand, Mongolia
- F1a1'4 – Thailand (Khon Mueang in Chiang Rai Province), China (Ma'an site, Wuxi, Majiabang culture)
- F1a1 – Japan, Korea, China, Ulchi, Uyghur, Vietnam (incl. Cờ Lao), Laos, Thailand, Indonesia, Mexico
- F1a1a – Thailand, Laos, Vietnam, China (Zhanjiang, etc.), Tibet, Indonesia
- F1a1a1 – Vietnam, Laos, Thailand, Cambodia, Nicobar Islands, Malaysia, Indonesia, China, Uyghur
- F1a1b – Japan, Korea
- F1a1c – Zhuang (Bama), Thailand, Tibet, Buryats (Inner Mongolia and Irkutsk Oblast), Japan
- F1a1c1 – Moken
- F1a1c2 – Japan, Xibo, China (Shanghai)
- F1a1d – Thailand, China, Taiwanese Aborigines (Tsou, Bunun, Rukai), Philippines
- F1a1d1 – Tao (Orchid Island)
- F1a1a – Thailand, Laos, Vietnam, China (Zhanjiang, etc.), Tibet, Indonesia
- F1a4
- F1a4a – Thailand, Han Chinese (Denver), Ulchi
- F1a4a1 – Taiwanese Aborigines (Tsou, Makatao, Bunun, Ami, etc.), Philippines (Ivatan, Ibaloi, Abaknon, Bugkalot, Kalangoya, Dulag, etc.), Guam, Malaysia (Kelantan Malay), Sumatra, Vietnam (Dao), Thailand (Khon Mueang in Mae Hong Son Province and Chiang Mai Province), South Africa
- F1a4b – China
- F1a4a – Thailand, Han Chinese (Denver), Ulchi
- F1a1 – Japan, Korea, China, Ulchi, Uyghur, Vietnam (incl. Cờ Lao), Laos, Thailand, Indonesia, Mexico
- F1a2 – Thailand, Vietnam (Hmong), China (Guizhou)
- F1a2a – Thailand (Phutai in Sakon Nakhon Province, Nyaw in Nakhon Phanom Province, Mon in Lopburi Province), China (Han in Zhanjiang, Dong, etc.)
- F1a3
- F1a3a – Philippines (Lipa City, Abaknon, Batak from Palawan Island, Aeta from Bataan), Taiwan, Indonesia
- F1a3a1 – Taiwan (Bunun, Puyuma, etc.)
- F1a3a1a – Japan, Korea
- F1a3a2 – Philippines (Ivatan)
- F1a3a3 – Taiwanese Aborigines (Tsou, Bunun, Makatao, Thao), Philippines (Ivatan)
- F1a3a7 - Philippines, Malaysia, Indonesia
- F1a3a8 - Philippines
- F1a3a1 – Taiwan (Bunun, Puyuma, etc.)
- F1a3b - China (Hunan Han, etc.), Taiwan (Minnan from Kaohsiung, etc.), Kazakhstan (Jetisu)
- F1a3c (C10223T) - Thailand (Khmer, etc.), China (Han)
- F1a3e (C11860T) - Thailand, China (Uyghurs)
- F1a3a – Philippines (Lipa City, Abaknon, Batak from Palawan Island, Aeta from Bataan), Taiwan, Indonesia
- F1a1'4 – Thailand (Khon Mueang in Chiang Rai Province), China (Ma'an site, Wuxi, Majiabang culture)
- F1c – Japan
- F1c1 – Japan
- F1c1a – Korea, Xinjiang, Tibet, Jammu and Kashmir, Thailand (Palaung in Chiang Mai Province, Khmu in Nan Province, Khon Mueang in Lampang Province)
- F1c1a1 – Russia, China (Qingdao, etc.), Evenk (New Barag Left Banner), Oroqen, Zhuang (Bama), Taiwan (Minnan)
- F1c1a1a – Tibet (Shannan, Sherpa, etc.), Yi
- F1c1a1b – China
- F1c1a2 – Tibet, Thailand, China (Chongqing), India
- F1c1a1 – Russia, China (Qingdao, etc.), Evenk (New Barag Left Banner), Oroqen, Zhuang (Bama), Taiwan (Minnan)
- F1c1a – Korea, Xinjiang, Tibet, Jammu and Kashmir, Thailand (Palaung in Chiang Mai Province, Khmu in Nan Province, Khon Mueang in Lampang Province)
- F1c1 – Japan
- F1f – Thailand, China, Lahu, Myanmar, Tibet, Cambodia, Vietnam (Hmong)
- F1a – China, Korea, Uyghur, Thailand, Mongolia
- F1-T16189C!
- F1b - Korea, Japan, Mongolia, China (North China)
- F1b1 – China, Tibet (Shigatse, etc.), Ladakh, Uyghur (Artux, etc.), Kyrgyz, Azeri, Kurd (Iran), Armenian, Turkey, Russia, Croatia
- F1b1a – Japan, Korea, Uyghur
- F1b1a1 – Japan, Korea
- F1b1a1a – Japan, Korea, USA (African American)
- F1b1a1a1 – Japan, Korea
- F1b1a1a1a – Japan
- F1b1a1a2 – Japan, Korea
- F1b1a1a3 – Japan
- F1b1a1a1 – Japan, Korea
- F1b1a1a – Japan, Korea, USA (African American)
- F1b1a2 – Japan, Korea
- F1b1a1 – Japan, Korea
- F1b1b – Yakut, Uyghur, Kyrgyz, Turk, Even (Sakkyryyr, Tompo), Korea
- F1b1c – China, Yi, Buryat
- F1b1d – Japan, Korea
- F1b1e – Uyghur, Kyrgyz, Buryat, Oroqen, Russian (Sverdlovsk Oblast)
- F1b1e1 – Yakut
- F1b1f – China, Uyghur, Buryat (Buryat Republic), Yakut (Namsky District), Evenk (Stony Tunguska River basin), Hungary (ancient Avars)
- F1b1a – Japan, Korea, Uyghur
- F1b1 – China, Tibet (Shigatse, etc.), Ladakh, Uyghur (Artux, etc.), Kyrgyz, Azeri, Kurd (Iran), Armenian, Turkey, Russia, Croatia
- F1d – China (Hunan, Zhejiang, Jiangsu, Beijing, Liaoning, Korean from Antu County, Hezhen, Minnan, Lhasa, etc.), Thailand (Mon in Kanchanaburi Province), South Korea, Japan, Kyrgyz (Artux, Ak-Say), ancient Scythian
- F1d1 – Tibet, Nepal (Tharu), Newar of Nepal (12%), Myanmar, Thailand (Mon in Kanchanaburi Province), China, Japan, South Africa
- F1e
- F1e1 – China (North China), Mongolia
- F1e1a – Japan
- F1e2 – China, Kyrgyz (Tashkurgan)
- F1e3 – China (Guangdong, etc.), Laos (Lao in Vientiane), Thailand (Phuan in Lopburi Province and Phichit Province), Sumatra, Vietnam (Kinh)
- F1e1 – China (North China), Mongolia
- F1g – Tibet, Thailand (Phuan in Lopburi Province, Sukhothai Province, and Phichit Province), China, Kyrgyz (Tashkurgan)
- F1g1 – China (Yunnan, etc.), Vietnam (Hmong, Dao), Nepal (Newar, 2.4%)
- F1b - Korea, Japan, Mongolia, China (North China)
- F1a'c'f – Thailand (Kaleun in Nakhon Phanom Province), China, Korea, Kazakhstan
- F2
- F2* – Laos (Lao in Vientiane), China, Hong Kong, Uyghur (Artux)
- F2a'b'g
- F2a – China (Han from Beijing, Xinjiang, etc.), Taiwan (Makatao), Korea, Japan, Kazakhstan
- F2a1 – China (Han from Shandong), Naxi, Bai, Nu, Tu (Monguor), Yi, Tibetan
- F2a2 – China (Han from Zhanjiang, etc.), Miao (Guizhou), Kinh (Guangxi), Dai and Lisu (Yunnan)
- F2a3 – China (Han from Xinjiang, Yunnan, Qinghai, and Shandong), Tu, Hui, Mongols in Inner Mongolia
- F2b – China (Han from Qingdao), Taiwan (Hakka)
- F2b1 – Thailand (Lao Isan in Roi Et Province and Chaiyaphum Province, Khon Mueang in Lampang Province), China (Han from Beijing, Xinjiang, etc.), Buryat (Irkutsk Oblast), Yakut, Even (NE Sakha Republic), Yukaghir (NE Sakha Republic), Nepal (Newar, 1.1%)
- F2g – China, Ladakh
- F2a – China (Han from Beijing, Xinjiang, etc.), Taiwan (Makatao), Korea, Japan, Kazakhstan
- F2c – China
- F2c1 – China (Shantou, etc.), Japan
- F2c2 – China (Han from Beijing), Kyrgyzstan (Kyrgyz)
- F2d – China, Uyghur, Thailand (Khon Mueang in Chiang Mai Province and Lamphun Province), Singapore, Japan, Kazakhstan
- F2e – China, Thailand (Tai Yuan in Uttaradit Province, Phuan in Phrae Province and Lopburi Province, Khon Mueang in Chiang Mai Province), Vietnam (Dao)
- F2e1 – China, Barghut (Hulun Buir)
- F2f – Japan, Korea, China, Pakistan (Hazara), Azerbaijan (Astara), Bashkortostan (Bashkir), Poland
- F2h'i – China
- F2h – China, Tibet (Lhasa), Taiwan, Thailand (Tai Dam in Kanchanaburi Province)
- F2i – China, Taiwan (Makatao), Korea
- F3 (formerly R9a)
- F3a – China (Han from Ili, etc.), Uyghur, Thailand
- F3a1 – China (Han from Yunnan, Guizhou, Shantou, Lanzhou,Hongbin Yao, Mengge Wang, Xing Zou, et al., "New insights into the fine-scale history of western-eastern admixture of the northwestern Chinese population in the Hexi Corridor via genome-wide genetic legacy." Mol Genet Genomics 2021 Mar 1. doi: 10.1007/s00438-021-01767-0. etc.), Kyrgyz (Tashkurgan), Taiwan (Hakka, etc.), Thailand (Phuan in Suphan Buri Province, Shan in Mae Hong Son Province, Khon Mueang in Chiang Rai Province, Mae Hong Son Province, Chiang Mai Province, Lamphun Province, and Lampang Province), Vietnam (Hmong, Dao)
- F3b – Thailand, Japan, Korea, China (Han from Qijiang), Yi
- F3b1 – Philippines, Comoros (Comorian from Grande Comore), USA
- F3b1a – Taiwan (Rukai, Puyuma, Paiwan, Tsou, Makatao, Bunun, Ami, etc.), Philippines (Maranao)
- F3b1a1 – Philippines (Bugkalot), Indonesia
- F3b1a2 – Taiwan (Puyuma, Bunun, Paiwan, etc.)
- F3b1b – Madagascar, Sumatra, Philippines (Batak from Palawan Island)
- F3b1b1 – Philippines (Ibaloi, Kankanaey, Ifugao), Spain, Denmark
- F3b1a – Taiwan (Rukai, Puyuma, Paiwan, Tsou, Makatao, Bunun, Ami, etc.), Philippines (Maranao)
- F3b1 – Philippines, Comoros (Comorian from Grande Comore), USA
- F3a – China (Han from Ili, etc.), Uyghur, Thailand
- F4
- F4a – Thailand/Laos, China, Taiwan, Korea
- F4a1
- F4a1a – Japan, China (Han from Lanzhou, She), Taiwan
- F4a1b – China, Japan
- F4a2 – China, Laos (Lao in Vientiane and Luang Prabang), Thailand (Phuan in Lopburi Province, Nyah Kur in Chaiyaphum Province, Khon Mueang in Lamphun Province)
- F4a1
- F4b – China (Han from Beijing), Thailand (Khon Mueang in Mae Hong Son Province, Lao Isan in Roi Et Province)
- F4b1 – China, Taiwan (Atayal, Bunun, Saisiyat, Thao, Tsou, Ami, Makatao, etc.), Philippines, Madagascar
- F4a – Thailand/Laos, China, Taiwan, Korea
Table of frequencies by ethnic group
| Population | Frequency | Count | Source | Subtypes | ||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Lahu (Lancang, Yunnan) | 0.771 | 35 | F1a=18, F(xF1a, F1b, F1c, F2a)=9 | |||||||||||||||||||||||||||||||||||||||
| Senoi (Malaysia) | 0.442 | 52 | vauthors=Hill C, Soares P, Mormina M, Macaulay V, Meehan W, Blackburn J, Clarke D, Raja JM, Ismail P, Bulbeck D, Oppenheimer S, Richards M | date=December 2006 | title=Phylogeography and ethnogenesis of aboriginal Southeast Asians | journal=Molecular Biology and Evolution | volume=23 | issue=12 | pages=2480–2491 | doi=10.1093/molbev/msl124 | pmid=16982817 | doi-access=free | hdl-access=free | hdl=1885/23220}} | F1a1a=23 | |||||||||||||||||||||||||||
| Tujia (Yongshun, Hunan) | 0.433 | 30 | F(xF1a, F1b, F1c, F2a)=6, F1a=4, F1c=2, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Shor (Kemerovo) | 0.415 | 82 | F1=33, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Lahu (Simao, Yunnan) | 0.344 | 32 | F1a=10, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Lahu (Xishuangbanna, Yunnan) | 0.333 | 15 | F1a=3, F1b=1, F1c=1 | |||||||||||||||||||||||||||||||||||||||
| Pan Yao (Tianlin, Guangxi) | 0.313 | 32 | vauthors=Wen B, Li H, Gao S, Mao X, Gao Y, Li F, Zhang F, He Y, Dong Y, Zhang Y, Huang W, Jin J, Xiao C, Lu D, Chakraborty R, Su B, Deka R, Jin L | date=March 2005 | title=Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages | journal=Molecular Biology and Evolution | volume=22 | issue=3 | pages=725–734 | doi=10.1093/molbev/msi055 | pmid=15548747 | doi-access=free}} | F3=2, F1b=2, F1a1a=2, F1a1(xF1a1a)=2, F1a(xF1a1)=1, F1c=1 | |||||||||||||||||||||||||||||
| Yi (Hezhang County, Guizhou) | 0.300 | 20 | F1b=4, F1a=2 | |||||||||||||||||||||||||||||||||||||||
| Lingao (Hainan) | 0.290 | 31 | F(xF1, F2, F3, F4)=2, F2=2, F1(xF1a)=1, F1a1(xF1a1a)=1, F1a1a=1, F3=1, F4=1 | |||||||||||||||||||||||||||||||||||||||
| Lowland Yao (Fuchuan, Guangxi) | 0.286 | 42 | F2a=4, F1a1(xF1a1a)=2, F1a(xF1a1)=2, F1b=1, F1c=1, F1(xF1a, F1b, F1c)=1, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Xiban Yao (Fangcheng, Guangxi) | 0.273 | 11 | F1b=1, F1a(xF1a1)=1, F(xF1, F2a, F3)=1 | |||||||||||||||||||||||||||||||||||||||
| Lanten Yao (Tianlin, Guangxi) | 0.269 | 26 | F1a(xF1a1)=5, F1a1(xF1a1a)=1, F(xF1, F2a, F3)=1 | |||||||||||||||||||||||||||||||||||||||
| Bai (Xishuangbanna, Yunnan) | 0.263 | 19 | F1a=2, F1b=2, F(xF1a, F1b, F1c, F2a)=1 | |||||||||||||||||||||||||||||||||||||||
| Huatou Yao (Fangcheng, Guangxi) | 0.263 | 19 | F1a1a=2, F1a1(xF1a1a)=1, F1a(xF1a1)=1, F(xF1, F2a, F3)=1 | |||||||||||||||||||||||||||||||||||||||
| Vietnamese | 0.262 | 42 | F1a=10, F(xF1a, F1b, F1c, F2)=1 | |||||||||||||||||||||||||||||||||||||||
| Taiwan (aborigines) | 0.253 | 640 | F4=72, F3=54, F1a1(xF1a1a)=21, F1a(xF1a1)=14, F2=1 | |||||||||||||||||||||||||||||||||||||||
| Bai (Dali, Yunnan) | 0.250 | 68 | F1a=6, F1c=4, F2a=4, F1b=2, F(xF1a, F1b, F1c, F2a)=1 | |||||||||||||||||||||||||||||||||||||||
| Indonesian (Mataram, Lombok) | 0.250 | 44 | F1a1a=4, F1a(xF1a1, F1a3, F1a4, F1a5)=4, F1a3=1, F1a4=1, F(xF1a, F1b, F2, F3a, F3b, F4)=1 | |||||||||||||||||||||||||||||||||||||||
| Uyghur (Uzbekistan/Kyrgyzstan) | 0.250 | 16 | vauthors=Comas D, Plaza S, Wells RS, Yuldaseva N, Lao O, Calafell F, Bertranpetit J | date=June 2004 | title=Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages | journal=European Journal of Human Genetics | volume=12 | issue=6 | pages=495–504 | doi=10.1038/sj.ejhg.5201160 | pmid=14872198 | doi-access=free}} | F=4 | |||||||||||||||||||||||||||||
| Yi (Xishuangbanna, Yunnan) | 0.250 | 16 | F1b=2, F1a=1, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Khakassian (Khakassia) | 0.246 | 57 | F1=11, F2a=3 | |||||||||||||||||||||||||||||||||||||||
| Naxi (Lijiang, Yunnan) | 0.244 | 45 | F1a=8, F1b=2, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Bunu (Dahua & Tianlin, Guangxi) | 0.240 | 25 | F1b=2, F(xF1, F2a, F3)=1, F1a1(xF1a1a)=1, F1a1a=1, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Ket | 0.237 | 38 | vauthors=Starikovskaya EB, Sukernik RI, Derbeneva OA, Volodko NV, Ruiz-Pesini E, Torroni A, Brown MD, Lott MT, Hosseini SH, Huoponen K, Wallace DC | date=January 2005 | title=Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups | journal=Annals of Human Genetics | volume=69 | issue=Pt 1 | pages=67–89 | doi=10.1046/j.1529-8817.2003.00127.x | pmc=3905771 | pmid=15638829}} | F=9 | |||||||||||||||||||||||||||||
| Han (Beijing) | 0.225 | 40 | F1a=4, F(xF1a, F1b, F1c, F2)=3, F1b=2 | |||||||||||||||||||||||||||||||||||||||
| Taiwanese (Taipei, Taiwan) | 0.220 | 91 | F=20 | |||||||||||||||||||||||||||||||||||||||
| Han (Southwest China; pool of 44 Sichuan, 34 Chongqing, 33 Yunnan, & 26 Guizhou) | 0.219 | 137 | F1a=15, F2=8, F3=7 | |||||||||||||||||||||||||||||||||||||||
| Hani (Xishuangbanna, Yunnan) | 0.212 | 33 | F1a=6, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Shigatse, Tibet) | 0.207 | 29 | F1a=5, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Tujia (Yanhe County, Guizhou) | 0.207 | 29 | F1a=2, F1c=1, F2a3=1, F2b=1, F(xF1, F2)=1 | |||||||||||||||||||||||||||||||||||||||
| Bapai Yao (Liannan, Guangdong) | 0.200 | 35 | F1b=3, F3=2, F1a1a=1, F1a(xF1a1)=1 | |||||||||||||||||||||||||||||||||||||||
| Indonesian (Waingapu, Sumba) | 0.200 | 50 | F1a4=3, F1a3=2, F1a1a=2, F1a(xF1a1, F1a3, F1a4, F1a5)=1, F1a1(xF1a1a)=1, F3b=1 | |||||||||||||||||||||||||||||||||||||||
| Manchurian | 0.200 | 40 | F(xF1a, F1b, F1c, F2)=3, F1a=2, F1b=2, F1c=1 | |||||||||||||||||||||||||||||||||||||||
| Thai | 0.200 | 40 | F1b=8 | |||||||||||||||||||||||||||||||||||||||
| Li (Hainan) | 0.197 | 346 | F1a1(xF1a1a)=30, F2=20, F1(xF1a)=4, F1a(xF1a1)=4, F1a1a=3, F3=3, F4=3, F(xF1, F2, F3, F4)=1 | |||||||||||||||||||||||||||||||||||||||
| Han (Xinjiang) | 0.191 | 47 | F1a=2, F3=2, F1b=1, F1c=1, F2a2=1, F2a3=1, F4=1 | |||||||||||||||||||||||||||||||||||||||
| Thailand | 0.190 | 105 | F1=18, F(xF1)=2 | |||||||||||||||||||||||||||||||||||||||
| Lisu (Gongshan, Yunnan) | 0.189 | 37 | F2a=4, F1b=2, F1a=1 | |||||||||||||||||||||||||||||||||||||||
| Han (southern California) | 0.187 | 390 | F=73 | |||||||||||||||||||||||||||||||||||||||
| Oirat Mongol (Xinjiang) | 0.184 | 49 | F2(xF2a2, F2a3, F2b)=3, F1b=3, F1a=2, F2b=1 | |||||||||||||||||||||||||||||||||||||||
| Dong (Tianzhu County, Guizhou) | 0.179 | 28 | F1a=4, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Han (Taiwan) | 0.175 | 1117 | F=196 | |||||||||||||||||||||||||||||||||||||||
| CHB (Han from Beijing Normal University) | 0.174 | 121 | F=21 | |||||||||||||||||||||||||||||||||||||||
| Jino (Xishuangbanna, Yunnan) | 0.167 | 18 | F1a=2, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Nu (Gongshan, Yunnan) | 0.167 | 30 | F2a=5 | |||||||||||||||||||||||||||||||||||||||
| Gelao (Daozhen County, Guizhou) | 0.161 | 31 | F1a=3, F1(xF1a, F1b, F1c)=1, F(xF1, F2)=1 | |||||||||||||||||||||||||||||||||||||||
| Nepal (Newar) | 0.155 | F1c1a = 2.4%, F1d = 12%, F1g = 2.4%, F2b1 = 1.1% | ||||||||||||||||||||||||||||||||||||||||
| CHD (Han from Denver) | 0.151 | 73 | F=11 | |||||||||||||||||||||||||||||||||||||||
| Filipino (Palawan) | 0.150 | 20 | F3b2=3 | |||||||||||||||||||||||||||||||||||||||
| Indonesian (52 Pekanbaru, 42 Medan, 34 Bangka, 28 Palembang, & 24 Padang) | 0.150 | 180 | F1a1a=9, F1a(xF1a1, F1a3, F1a4, F1a5)=8, F1a5=3, F4=3, F1a3=2, F1a4=2 | |||||||||||||||||||||||||||||||||||||||
| Kyrgyz (Uzbekistan/Kyrgyzstan) | 0.150 | 20 | F=3 | |||||||||||||||||||||||||||||||||||||||
| Yi (Shuangbai, Yunnan) | 0.150 | 40 | F(xF1a, F1b, F1c, F2a)=2, F1a=2, F1b=2 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Ulan Bator) | 0.149 | 47 | F1a=3, F1b=3, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Borneo (89 Banjarmasin & 68 Kota Kinabalu) | 0.146 | 157 | F3b=9, F(xF1a, F1b, F2, F3a, F3b, F4)=4, F1a3=3, F1a4=3, F1a1(xF1a1a)=2, F1a(xF1a1, F1a3, F1a4, F1a5)=1, F1a1a=1 | |||||||||||||||||||||||||||||||||||||||
| Indonesian (Bali) | 0.146 | 82 | F1a(xF1a1, F1a3, F1a4, F1a5)=5, F1a1(xF1a1a)=4, F1a1a=2, F(xF1a, F1b, F2, F3a, F3b, F4)=1 | |||||||||||||||||||||||||||||||||||||||
| Hmong (Jishou, Hunan) | 0.146 | 103 | F1a1(xF1a1a)=4, F1a1a=3, F(xF1, F2a, F3)=3, F1a(xF1a1)=2, F1b=2, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Aini (Xishuangbanna, Yunnan) | 0.140 | 50 | F1a=6, F(xF1a, F1b, F1c, F2a)=1 | |||||||||||||||||||||||||||||||||||||||
| Indonesian (Ambon) | 0.140 | 43 | F1a3=3, F1a4=2, F1a1a=1 | |||||||||||||||||||||||||||||||||||||||
| Cun (Hainan) | 0.133 | 30 | F4=3, F1a1(xF1a1a)=1 | |||||||||||||||||||||||||||||||||||||||
| Hui (Xinjiang) | 0.133 | 45 | F1b=2, F1c=2, F1a=1, F2a3=1 | |||||||||||||||||||||||||||||||||||||||
| Batak (Palawan) | 0.129 | 31 | F1a3=3, F3b2=1 | |||||||||||||||||||||||||||||||||||||||
| Yi (Luxi, Yunnan) | 0.129 | 31 | F1b=3, F(xF1a, F1b, F1c, F2a)=1 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Khovd Province) | 0.128 | 429 | F(xF1e1a)=7, F1=3, F1a=2, F1a1=4, F1a1a(xF1a1a1)=4, F1a2=2, F1b=2, F1b1(xF1b1b)=5, F2=1, F2a=14, F2b1=4, F4a=7 | |||||||||||||||||||||||||||||||||||||||
| Guoshan Yao (Jianghua, Hunan) | 0.125 | 24 | F1a(xF1a1)=1, F1b=1, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Tu Yao (Hezhou, Guangxi) | 0.122 | 41 | F1a1a=4, F1a(xF1a1)=1 | |||||||||||||||||||||||||||||||||||||||
| Gelao (Daozhen County, Guizhou) | 0.118 | 102 | F1a(xF1a1)=4, F1b=3, F2(xF2a, F2b)=2, F3a=2, F3(xF3a)=1 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Nagchu, Tibet) | 0.114 | 35 | F=4 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Lhasa, Tibet) | 0.114 | 44 | F1a=2, F2=2, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Filipino (Luzon) | 0.113 | 177 | vauthors=Tabbada KA, Trejaut J, Loo JH, Chen YM, Lin M, Mirazón-Lahr M, Kivisild T, De Ungria MC | date=January 2010 | title=Philippine mitochondrial DNA diversity: a populated viaduct between Taiwan and Indonesia? | journal=Molecular Biology and Evolution | volume=27 | issue=1 | pages=21–31 | doi=10.1093/molbev/msp215 | pmid=19755666 | doi-access=free}} | F1a3=6, F1a4=6, F3b=5, F4b=2, F1a1a=1 | |||||||||||||||||||||||||||||
| Indonesian (Alor) | 0.111 | 45 | F1a4=3, F1a1a=1, F1a(xF1a1, F1a3, F1a4, F1a5)=1 | |||||||||||||||||||||||||||||||||||||||
| Indonesian (Sulawesi, incl. 89 Manado, 64 Toraja, 46 Ujung Padang, & 38 Palu) | 0.110 | 237 | F1a4=12, F1a3=4, F1a(xF1a1, F1a3, F1a4, F1a5)=4, F1a1a=3, F1a1(xF1a1a)=1, F1a5=1, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Tujia (western Hunan) | 0.109 | 64 | F(xF1a, F1b, F1c, F2a)=2, F1a=2, F1b=2, F1c=1 | |||||||||||||||||||||||||||||||||||||||
| Cham (Bình Thuận, Vietnam) | 0.107 | 168 | vauthors=Peng MS, Quang HH, Dang KP, Trieu AV, Wang HW, Yao YG, Kong QP, Zhang YP | date=October 2010 | title=Tracing the Austronesian footprint in Mainland Southeast Asia: a perspective from mitochondrial DNA | journal=Molecular Biology and Evolution | volume=27 | issue=10 | pages=2417–2430 | doi=10.1093/molbev/msq131 | pmid=20513740 | doi-access=free}} | F1a1a=10, F1(xF1a)=3, F1a(xF1a1)=3, F1a1(xF1a1a)=2 | |||||||||||||||||||||||||||||
| Tibetan (Shannan, Tibet) | 0.105 | 19 | F=2 | |||||||||||||||||||||||||||||||||||||||
| Altai Kizhi (Altai Republic) | 0.102 | 324 | vauthors = Dulik MC, Zhadanov SI, Osipova LP, Askapuli A, Gau L, Gokcumen O, Rubinstein S, Schurr TG | title = Mitochondrial DNA Dulik_2012 Y chromosome variation provides evidence for a recent common ancestry between Native Americans and Indigenous Altaians | journal = American Journal of Human Genetics | volume = 90 | issue = 2 | pages = 229–46 | date = February 2012 | pmid = 22281367 | doi = 10.1016/j.ajhg.2011.12.014 | pmc = 3276666 }} | F1=25, F2=8 | |||||||||||||||||||||||||||||
| Dingban Yao (Mengla, Yunnan) | 0.100 | 10 | F1a(xF1a1)=1 | |||||||||||||||||||||||||||||||||||||||
| Filipino (Visayas) | 0.098 | 112 | F1a4=7, F1a3=3, F3b=1 | |||||||||||||||||||||||||||||||||||||||
| Korean (South Korea) | 0.097 | 185 | F1a=8, F1b=8, F2(xF2a)=2 | |||||||||||||||||||||||||||||||||||||||
| Korean (Seoul National University Hospital) | 0.097 | 1365 | F=132 | |||||||||||||||||||||||||||||||||||||||
| Altai people (Altai Republic) | 0.095 | 726 | F1=44, F2=25 | |||||||||||||||||||||||||||||||||||||||
| Filipino | 0.094 | 64 | F1a3=3, F1a4=3 | |||||||||||||||||||||||||||||||||||||||
| Mien (Shangsi, Guangxi) | 0.094 | 32 | F1a1(xF1a1a)=2, F1a1a=1 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Tibet) | 0.093 | 216 | F1a=13, F1b=4, F2=3 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Mongolia) | 0.092 | 2420 | F1a=55, F1b=71, F1c=13, F1(xF1d, F1e1)=33, F2=44, F3a=2, F4a=7 | |||||||||||||||||||||||||||||||||||||||
| CHS (Han from Hunan & Fujian) | 0.091 | 55 | F=5 | |||||||||||||||||||||||||||||||||||||||
| Altai (Altai Republic) | 0.091 | 110 | F=10 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Khentii Province) | 0.091 | 132 | F1=1, F1a=3, F1b=5, F1c=2, F2b=1 | |||||||||||||||||||||||||||||||||||||||
| Buryat | 0.087 | 126 | F1b=6, F1a=3, F(xF1a, F1b, F1c, F2a)=2 | |||||||||||||||||||||||||||||||||||||||
| Tofalar | 0.087 | 46 | F1b=4 | |||||||||||||||||||||||||||||||||||||||
| Uzbek (Xinjiang) | 0.086 | 58 | F2a3=2, F4=2, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Tuvinian (Tuva) | 0.086 | 105 | F1=8, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Korean (South Korea) | 0.083 | 850 | F1a(xF1a3)=7, F1a1=17, F1b1=19, F1(xF1c, F1d)=11, F2=14, F3a=2, F4a1a=1 | |||||||||||||||||||||||||||||||||||||||
| Japanese (Tōhoku) | 0.083 | 336 | F=28 | |||||||||||||||||||||||||||||||||||||||
| Mongol (New Barag Left Banner) | 0.083 | 48 | F1a=2, F1c=1, F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Pumi (Ninglang, Yunnan) | 0.083 | 36 | F2a=2, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Diqing, Yunnan) | 0.083 | 24 | F1a=1, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Korean (South Korea) | 0.080 | 593 | F=3, F1=7, F1ac=2, F1a=12, F1c=2, F1b=16, F2a=3 | |||||||||||||||||||||||||||||||||||||||
| Korean (Ulsan) | 0.079 | 1094 | F=86 | |||||||||||||||||||||||||||||||||||||||
| Korean (northern China) | 0.078 | 51 | F(xF1a, F1b, F1c, F2)=1, F1a=1, F1b=1, F1c=1 | |||||||||||||||||||||||||||||||||||||||
| Daur (Hulunbuir) | 0.076 | 209 | F1a=2, F1a1(xF1a1a)=4, F1a1a1=1, F1b1(xF1b1b)=2, F1c1a=1, F2(xF2d)=5, F4a1b=1 | |||||||||||||||||||||||||||||||||||||||
| JPT (Japanese from Tokyo) | 0.076 | 118 | F=9 | |||||||||||||||||||||||||||||||||||||||
| Kazakh (Xinjiang) | 0.075 | 53 | F1b=3, F2(xF2a2, F2a3, F2b)=1 | |||||||||||||||||||||||||||||||||||||||
| Chinese (Shenyang, Liaoning) | 0.075 | 160 | F=12 | |||||||||||||||||||||||||||||||||||||||
| Danga (Hainan) | 0.075 | 40 | F1a1(xF1a1a)=1, F2=1, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Japanese (northern Kyūshū) | 0.074 | 256 | F=19 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Nyingchi, Tibet) | 0.074 | 54 | F1a=2, F1b=2 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Sükhbaatar Province) | 0.073 | 246 | F=1, F1a=5, F1b=8, F1c=3, F2i=1 | |||||||||||||||||||||||||||||||||||||||
| Uyghur | 0.073 | 55 | F1b=2, F1a=1, F1c=1 | |||||||||||||||||||||||||||||||||||||||
| Filipino (Mindanao) | 0.071 | 70 | F3b=2, F1a4=2, F1a3=1 | |||||||||||||||||||||||||||||||||||||||
| Korean (Seoul & Daejeon, South Korea) | 0.069 | 261 | F1=12, F(xF1)=6 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Chamdo, Tibet) | 0.069 | 29 | F1a=2 | |||||||||||||||||||||||||||||||||||||||
| Semelai (Malaysia) | 0.066 | 61 | F1a1a=4 | |||||||||||||||||||||||||||||||||||||||
| Japanese (Hokkaidō) | 0.065 | 217 | F=14 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Dornod Province) | 0.065 | 370 | F1(xF1c, F1d)=6, F1a=7, F1b=7, F2=4 | |||||||||||||||||||||||||||||||||||||||
| Wuzhou Yao (Fuchuan, Guangxi) | 0.065 | 31 | F1a1(xF1a1a)=1, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Korean (South Korea) | 0.064 | 203 | F=13 | |||||||||||||||||||||||||||||||||||||||
| Mongolian (Ulan Bator) | 0.064 | 47 | F1=3 | |||||||||||||||||||||||||||||||||||||||
| Uyghur (Xinjiang) | 0.064 | 47 | F1b=2, F1a=1 | |||||||||||||||||||||||||||||||||||||||
| Bashkir (Beloretsky, Sterlibashevsky, Ilishevsky, & Perm) | 0.063 | 221 | F=14 | |||||||||||||||||||||||||||||||||||||||
| Dungan (Uzbekistan/Kyrgyzstan) | 0.063 | 16 | F=1 | |||||||||||||||||||||||||||||||||||||||
| Japanese (Miyazaki) | 0.060 | 100 | vauthors=Taketo U, Rinnosuke H, Kenshi S, Kazuhiko I, Kazumasa S, Kentaro K | year=2007 | title=Mitochondrial DNA Sequence Variation and Phylogenetic Analysis in Japanese Individuals from Miyazaki Prefecture | journal=Japanese Journal of Forensic Science and Technology | volume=12 | issue=1 | pages=83–96 | doi=10.3408/jafst.12.83 | doi-access=free}} | F1b=3, F1a=2, F2a=1 | ||||||||||||||||||||||||||||||
| Kazakh (Zhetysu) | 0.060 | 200 | F1=11, F2=1 | |||||||||||||||||||||||||||||||||||||||
| Tharu (Chitwan, Nepal) | 0.060 | 133 | F1c=7, F1(xF1c, F1d)=1 | |||||||||||||||||||||||||||||||||||||||
| Japanese (Gifu) | 0.059 | 1617 | vauthors=Fuku N, Park KS, Yamada Y, Nishigaki Y, Cho YM, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Nozawa Y, Lee HK, Tanaka M | date=March 2007 | title=Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians | journal=American Journal of Human Genetics | volume=80 | issue=3 | pages=407–415 | doi=10.1086/512202 | pmc=1821119 | pmid=17273962}} | F=96 | |||||||||||||||||||||||||||||
| Japanese (Tōkai) | 0.057 | 282 | F=16 | |||||||||||||||||||||||||||||||||||||||
| Teleut (Kemerovo) | 0.057 | 53 | F1=3 | |||||||||||||||||||||||||||||||||||||||
| Altai Kizhi | 0.056 | 90 | F1=3, F2a=2 | |||||||||||||||||||||||||||||||||||||||
| Kalmyk (Kalmykia) | 0.055 | 110 | F1=6 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Shannan, Tibet) | 0.055 | 55 | F1a=2, F2=1 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Qinghai) | 0.054 | 56 | F1c=2, F1a=1 | |||||||||||||||||||||||||||||||||||||||
| Japanese | 0.052 | 211 | vauthors=Maruyama S, Minaguchi K, Saitou N | date=August 2003 | title=Sequence polymorphisms of the mitochondrial DNA control region and phylogenetic analysis of mtDNA lineages in the Japanese population | journal=International Journal of Legal Medicine | volume=117 | issue=4 | pages=218–225 | doi=10.1007/s00414-003-0379-2 | pmid=12845447 | s2cid=1224295}} | F1b=9, F1a=2 | |||||||||||||||||||||||||||||
| Hmong (Wenshan, Yunnan) | 0.051 | 39 | F1b=1, F3=1 | |||||||||||||||||||||||||||||||||||||||
| Kazakh (Kosh-Agach, Altai Republic) | 0.051 | 98 | vauthors=Derenko M, Malyarchuk B, Denisova G, Perkova M, Rogalla U, Grzybowski T, Khusnutdinova E, Dambueva I, Zakharov I | year=2012 | title=Complete mitochondrial DNA analysis of eastern Eurasian haplogroups rarely found in populations of northern Asia and eastern Europe | journal=PLOS ONE | volume=7 | issue=2 | article-number=e32179 | bibcode=2012PLoSO...732179D | doi=10.1371/journal.pone.0032179 | pmc=3283723 | pmid=22363811 | doi-access=free}} | F1=5 | |||||||||||||||||||||||||||
| Karakalpak (Uzbekistan/Kyrgyzstan) | 0.050 | 20 | F=1 | |||||||||||||||||||||||||||||||||||||||
| Tharu (Morang, Nepal) | 0.050 | 40 | F1c=1, F1d=1 | |||||||||||||||||||||||||||||||||||||||
| Turkmen (Uzbekistan/Kyrgyzstan) | 0.050 | 20 | F=1 | |||||||||||||||||||||||||||||||||||||||
| Korean (South Korea) | 0.049 | 103 | F1=5 | |||||||||||||||||||||||||||||||||||||||
| Oroqen (Oroqen Autonomous Banner) | 0.045 | 44 | F1b=2 | |||||||||||||||||||||||||||||||||||||||
| Yakut | 0.043 | 117 | F2a=3, F1b=2 | |||||||||||||||||||||||||||||||||||||||
| Tuvan | 0.042 | 95 | F(xF1b)=3, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Kyrgyz (Talas) | 0.042 | 48 | F1a=1, F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Nyingchi, Tibet) | 0.042 | 24 | F=1 | |||||||||||||||||||||||||||||||||||||||
| Khamnigan (Buryatia) | 0.040 | 99 | F1=4 | |||||||||||||||||||||||||||||||||||||||
| Iu Mien (Mengla, Yunnan) | 0.037 | 27 | F(xF1, F2a, F3)=1 | |||||||||||||||||||||||||||||||||||||||
| Kazakh | 0.036 | 55 | F1b=2 | |||||||||||||||||||||||||||||||||||||||
| Barghut (Hulunbuir) | 0.034 | 149 | F1=4, F2=1 | |||||||||||||||||||||||||||||||||||||||
| Buryat (Buryatia) | 0.031 | 295 | F1=7, F2a=2 | |||||||||||||||||||||||||||||||||||||||
| Ulch people | 0.031 | 160 | F1a=5 | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Zhongdian, Yunnan) | 0.029 | 35 | F2a=1 | |||||||||||||||||||||||||||||||||||||||
| Kim Mun (Malipo, Yunnan) | 0.025 | 40 | F1a1(xF1a1a)=1 | |||||||||||||||||||||||||||||||||||||||
| Uzbek (Uzbekistan/Kyrgyzstan) | 0.025 | 40 | F=1 | |||||||||||||||||||||||||||||||||||||||
| Okinawa | 0.025 | 326 | F=8 | |||||||||||||||||||||||||||||||||||||||
| Evenk (New Barag Left Banner) | 0.021 | 47 | F1c=1 | |||||||||||||||||||||||||||||||||||||||
| Ainu | 0.020 | 51 | F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Evenk (53 Stony Tunguska basin & 18 Tugur-Chumikan) | 0.014 | 71 | F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Telenghit (Altai Republic) | 0.014 | 71 | F1=1 | |||||||||||||||||||||||||||||||||||||||
| Tubalar | 0.014 | 72 | F1b=1 | |||||||||||||||||||||||||||||||||||||||
| Evenk (Krasnoyarsk) | 0.014 | 73 | F1=1 | |||||||||||||||||||||||||||||||||||||||
| Ulchi (Old & New Bulava, Ulchsky, Khabarovsk) | 0.011 | 87 | F(xF1b)=1 | |||||||||||||||||||||||||||||||||||||||
| Mansi | 0.010 | 98 | F=1 | |||||||||||||||||||||||||||||||||||||||
| Khanty | 0.009 | 106 | F1=1 | |||||||||||||||||||||||||||||||||||||||
| Turkish people | 0.004 | 773 | last1=Kars | first1=M. Ece | last2=Başak | first2=A. Nazlı | last3=Onat | first3=O. Emre | last4=Bilguvar | first4=Kaya | last5=Choi | first5=Jungmin | last6=Itan | first6=Yuval | last7=Çağlar | first7=Caner | last8=Palvadeau | first8=Robin | last9=Casanova | first9=Jean-Laurent | last10=Cooper | first10=David N. | last11=Stenson | first11=Peter D. | last12=Yavuz | first12=Alper | last13=Buluş | first13=Hakan | last14=Günel | first14=Murat | last15=Friedman | first15=Jeffrey M. | date=2021-09-07 | title=The genetic structure of the Turkish population reveals high levels of variation and admixture | journal=Proceedings of the National Academy of Sciences | volume=118 | issue=36 | article-number=e2026076118 | doi=10.1073/pnas.2026076118 | doi-access=free | pmc=8433500}} | F1b1+@152=1, F1b1e=1, F1b1f=1 |
| Chukchi (Anadyr) | 0.000 | 15 | - | |||||||||||||||||||||||||||||||||||||||
| Bukharan Arab (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |||||||||||||||||||||||||||||||||||||||
| Crimean Tatar (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |||||||||||||||||||||||||||||||||||||||
| Iranian (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |||||||||||||||||||||||||||||||||||||||
| Kazakh (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |||||||||||||||||||||||||||||||||||||||
| Tajik (Uzbekistan/Kyrgyzstan) | 0.000 | 20 | - | |||||||||||||||||||||||||||||||||||||||
| Hindu (Chitwan, Nepal) | 0.000 | 24 | - | |||||||||||||||||||||||||||||||||||||||
| Nganasan | 0.000 | 24 | - | |||||||||||||||||||||||||||||||||||||||
| Buryat (Kushun, Nizhneudinsk, Irkutsk Oblast) | 0.000 | 25 | - | |||||||||||||||||||||||||||||||||||||||
| Kurd (northwestern Iran) | 0.000 | 25 | - | |||||||||||||||||||||||||||||||||||||||
| Andhra Pradesh (tribal) | 0.000 | 29 | - | |||||||||||||||||||||||||||||||||||||||
| Batek (Malaysia) | 0.000 | 29 | - | |||||||||||||||||||||||||||||||||||||||
| Mendriq (Malaysia) | 0.000 | 32 | - | |||||||||||||||||||||||||||||||||||||||
| Negidal | 0.000 | 33 | - | |||||||||||||||||||||||||||||||||||||||
| Temuan (Malaysia) | 0.000 | 33 | - | |||||||||||||||||||||||||||||||||||||||
| Yakut (Yakutia) | 0.000 | 36 | - | |||||||||||||||||||||||||||||||||||||||
| Tibetan (Deqin, Yunnan) | 0.000 | 40 | - | |||||||||||||||||||||||||||||||||||||||
| Tajik (Tajikistan) | 0.000 | 44 | - | |||||||||||||||||||||||||||||||||||||||
| Daur (Evenk Autonomous Banner) | 0.000 | 45 | - | |||||||||||||||||||||||||||||||||||||||
| Evenk (Buryatia) | 0.000 | 45 | - | |||||||||||||||||||||||||||||||||||||||
| Udege (Gvasiugi, Imeni Lazo, Khabarovsk) | 0.000 | 46 | - | |||||||||||||||||||||||||||||||||||||||
| Itelmen | 0.000 | 47 | - | |||||||||||||||||||||||||||||||||||||||
| Kyrgyz (Sary-Tash) | 0.000 | 47 | - | |||||||||||||||||||||||||||||||||||||||
| Korean (Arun Banner) | 0.000 | 48 | - | |||||||||||||||||||||||||||||||||||||||
| Jahai (Malaysia) | 0.000 | 51 | - | |||||||||||||||||||||||||||||||||||||||
| Nivkh (northern Sakhalin) | 0.000 | 56 | - | |||||||||||||||||||||||||||||||||||||||
| Mansi | 0.000 | 63 | - | |||||||||||||||||||||||||||||||||||||||
| Chukchi | 0.000 | 66 | - | |||||||||||||||||||||||||||||||||||||||
| Siberian Eskimo | 0.000 | 79 | - | |||||||||||||||||||||||||||||||||||||||
| Persian (eastern Iran) | 0.000 | 82 | - | |||||||||||||||||||||||||||||||||||||||
| Koryak | 0.000 | 155 | - |
References
References
- (June 2009). "Correcting for purifying selection: an improved human mitochondrial molecular clock". American Journal of Human Genetics.
- (February 2009). "Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation". Human Mutation.
- [http://www.ianlogan.co.uk/discussion/hap_F.htm Haplogroup F.]
- (November 2007). "Phylogeographic analysis of mitochondrial DNA in northern Asian populations". American Journal of Human Genetics.
- M. A. Bermisheva, K. Tambets, R. Villems, and E. K. Khusnutdinova, "Diversity of Mitochondrial DNA Haplogroups in Ethnic Populations of the Volga–Ural Region", ''Molecular Biology'' Vol. 36, No. 6, 2002, pp. 802–812. Translated from ''Molekulyarnaya Biologiya'', Vol. 36, No. 6, 2002, pp. 990–1001.
- (July 2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation". BMC Evolutionary Biology.
- (October 2008). "Northwest Siberian Khanty and Mansi in the junction of West and East Eurasian gene pools as revealed by uniparental markers". European Journal of Human Genetics.
- (January 2011). "Genetic diversity on the Comoros Islands shows early seafaring as major determinant of human biocultural evolution in the Western Indian Ocean". European Journal of Human Genetics.
- (September 2001). "The evidence of mtDNA haplogroup F in a European population and its ethnohistoric implications". European Journal of Human Genetics.
- (February 2023). "The matrilineal ancestry of Nepali populations". Human Genetics.
- (May 2004). "Analyses of genetic structure of Tibeto-Burman populations reveals sex-biased admixture in southern Tibeto-Burmans". American Journal of Human Genetics.
- Hwan Young Lee, Ji-Eun Yoo, Myung Jin Park, Ukhee Chung, Chong-Youl Kim, and Kyoung-Jin Shin, "East Asian mtDNA haplogroup determination in Koreans: Haplogroup-level coding region SNP analysis and subhaplogroup-level control region sequence analysis." ''Electrophoresis'' (2006). DOI 10.1002/elps.200600151.
- Wibhu Kutanan, Jatupol Kampuansai, Metawee Srikummool, Daoroong Kangwanpong, Silvia Ghirotto, Andrea Brunelli, and Mark Stoneking, "Complete mitochondrial genomes of Thai and Lao populations indicate an ancient origin of Austroasiatic groups and demic diffusion in the spread of Tai–Kadai languages." ''Hum Genet'' 2016 DOI 10.1007/s00439-016-1742-y.
- (2022). "Mitochondrial DNA Footprints from Western Eurasia in Modern Mongolia". Frontiers in Genetics.
- Rebecca S Just, Melissa K Scheible, Spence A Fast, ''et al.'', "Full mtGenome reference data: development and characterization of 588 forensic-quality haplotypes representing three U.S. populations." ''Forensic Sci Int Genet.'' 2015 Jan;14:141-55. doi: 10.1016/j.fsigen.2014.09.021. Epub 2014 Oct 5.
- Kong, Q.P., Yao, Y.G., Sun, C., Zhu, C.L., Zhong, L., Wang, C.Y., Cai, W.W., Xu, X.M., Xu, A.L. and Zhang, Y.P., 2004. Phylogeographic analysis of mitochondrial DNA haplogroup F2 in China reveals T12338C in the initiation codon of the ND5 gene not to be pathogenic. Journal of human genetics, 49(8), p.414.
- Sardana A Fedorova, Maere Reidla, Ene Metspalu, ''et al.'', "Autosomal and uniparental portraits of the native populations of Sakha (Yakutia): implications for the peopling of Northeast Eurasia." ''BMC Evolutionary Biology'' 2013, 13:127. http://www.biomedcentral.com/1471-2148/13/127
- (December 2006). "Phylogeography and ethnogenesis of aboriginal Southeast Asians". Molecular Biology and Evolution.
- (March 2005). "Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages". Molecular Biology and Evolution.
- (June 2004). "Admixture, migrations, and dispersals in Central Asia: evidence from maternal DNA lineages". European Journal of Human Genetics.
- (January 2005). "Mitochondrial DNA diversity in indigenous populations of the southern extent of Siberia, and the origins of Native American haplogroups". Annals of Human Genetics.
- Supannee Kaewsutthi, Nopasak Phasukkijwatana, Yutthana Joyjinda ''et al.'', "Mitochondrial Haplogroup Background May Influence Southeast Asian G11778A Leber Hereditary Optic Neuropathy", ''Investigative Ophthalmology & Visual Science'', June 2011, Vol. 52, No. 7
- (January 2010). "Philippine mitochondrial DNA diversity: a populated viaduct between Taiwan and Indonesia?". Molecular Biology and Evolution.
- (October 2010). "Tracing the Austronesian footprint in Mainland Southeast Asia: a perspective from mitochondrial DNA". Molecular Biology and Evolution.
- (February 2012). "Mitochondrial DNA Dulik_2012 Y chromosome variation provides evidence for a recent common ancestry between Native Americans and Indigenous Altaians". American Journal of Human Genetics.
- (March 2007). "Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians". American Journal of Human Genetics.
- D Miścicka-Sliwka, M Woźniak, I A Zakharov. (2003). "Diversity of mitochondrial DNA lineages in South Siberia". Annals of Human Genetics.
- Yoo, Seong-Keun. (2019). "Northeast Asian Reference Database (NARD) Imputation Server".
- (2006). "East Asian mtDNA haplogroup determination in Koreans: Haplogroup-level coding region SNP analysis and subhaplogroup-level control region sequence analysis". Electrophoresis.
- (May 2020). "Korean Genome Project: 1094 Korean personal genomes with clinical information". Science Advances.
- Chi-Zao Wang, Xue-Er Yu, Mei-Sen Shi, Hui Li & Shu-Hua Ma. (2022). "Whole mitochondrial genome analysis of the Daur ethnic minority from Hulunbuir in the Inner Mongolia Autonomous Region of China". BMC Ecology and Evolution.
- (2007). "Mitochondrial DNA Sequence Variation and Phylogenetic Analysis in Japanese Individuals from Miyazaki Prefecture". Japanese Journal of Forensic Science and Technology.
- Ayken Askapuli, Miguel Vilar, Humberto Garcia-Ortiz. (2022). "Kazak mitochondrial genomes provide insights into the human population history of Central Eurasia". PLOS ONE.
- (March 2007). "Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians". American Journal of Human Genetics.
- (August 2003). "Sequence polymorphisms of the mitochondrial DNA control region and phylogenetic analysis of mtDNA lineages in the Japanese population". International Journal of Legal Medicine.
- (2012). "Complete mitochondrial DNA analysis of eastern Eurasian haplogroups rarely found in populations of northern Asia and eastern Europe". PLOS ONE.
- (2021-09-07). "The genetic structure of the Turkish population reveals high levels of variation and admixture". Proceedings of the National Academy of Sciences.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Haplogroup F (mtDNA) — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report