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Haplogroup E-Z827
Human Y-chromosome DNA haplogroup
Human Y-chromosome DNA haplogroup
| Field | Value |
|---|---|
| name | E-Z827 |
| origin-place | Middle East |
| origin-date | 23,900 BP |
| TMRCA | 23,500 BP |
| ancestor | E-M35 |
| descendants | E-L19, E-Z830 |
| mutations | Z827 / CTS1243, Y473649, CTS7890 / M5239, M5323 / S24409, Y501567(H); Y506656(H), Y506929(H), Y603505(H), Y501568(H), Y468887(H), Y491119, S25930(H) |
| origin-place = Middle East | origin-date = 23,900 BP E-Z827, also known as E1b1b1b, is a major human Y-chromosome DNA haplogroup. It is the parent lineage to the E-Z830 and E-L19subclades, and defines their common phylogeny. The former is predominantly found in East Africa; the latter is most frequently around the Mediterannean Sea,. E-Z827 is also found at lower frequencies in Europe, and in isolated parts of Southeast Africa.
Subclades of E-Z827 and Distribution
Family Tree
The following phylogeny is based on the YCC 2008 tree and subsequent published research as summarized by ISOGG.
- E-Z827 (Z827) - E1b1b1b
- E-L19 (L19) - E1b1b1b1
- E-PF2431 (PF2431)
- E-PF2438
- E-Y10561
- E-FGC18981
- E-FGC38527
- E-Y35933
- E-FGC18960
- E-Y33020
- E-FGC18958
- E-FGC18981
- E-PF2440
- E-PF2471
- E-BY9805
- E-PF2471
- E-Y10561
- E-PF2438
- E-M81 (M81)
- E-M81*
- E-M165 - Found only in Israel and Germany.
- E-Y596059 - Found only in Iraq.
- E-CTS4236 - Found only in Syria.
- E-CTS6256 - Found in Europe and North Africa.
- E-PF2548
- E-PF2546
- E-PF2546*
- E-CTS12227
- E-MZ11
- E-MZ12
- E-MZ11
- E-A929
- E-Z5009
- E-Z5009*
- E-Z5010
- E-Z5013
- E-Z5013*
- E-A1152
- E-A2227
- E-A428
- E-MZ16
- E-PF6794
- E-PF6794*
- E-PF6789
- E-MZ21
- E-MZ23
- E-MZ80
- E-A930
- E-Z2198/E-MZ46
- E-A601
- E-L351
- E-Z5009
- E-PF2546
- E-PF2548
- E-CTS6256 - Found in Europe and North Africa.
- E-PF2431 (PF2431)
- E-Z830 (Z830) - E1b1b1b2
- E-M123 (M123)
- E-M34 (M34)
- E-M84 (M84)
- E-M136 (M136)
- E-M290 (M290)
- E-V23 (V23)
- E-L791 (L791,L792)
- E-M84 (M84)
- E-M34 (M34)
- E-V1515
- E-V1515*
- E-V1486
- E-V1486*
- E-V2881
- E-V2881*
- E-V1792
- E-V92
- E-M293 (M293)
- E-M293*
- E-P72 (P72)
- E-V3065*
- E-V1700
- E-V42 (V42)
- E-V1785
- E-V1785*
- E-V6 (V6)
- E-M123 (M123)
- E-L19 (L19) - E1b1b1b1
E-L19 (E1b1b1b1)

To date, only two immediate downstream subclades of E-L19 have been recognized: E-PF2431 and E-M81.
'''E-M81'''
E-M81 is the dominant subclade of E-L19, accounting for more than 99% of its carriers. It has three main branches: E-M165, carried exclusively by a German and an Israeli; E-Y596059, carried by a Syrian from Damascus and an Iraqi Al Anbar; and E-CTS4236, carried exclusively by a Syrian from Quneitra, nearly all branches of E-M81 today derives from E-CTS4236. It is thought to have originated in the Near East, roughly 13,000 years ago, with subsequent expansions into Europe and North Africa occurring either about 1,000 years ago via Arab populations or around 3,000 years ago through Phoenician movements.This distribution has been usually explained as a consequence of a westward expansion from the Near East and this event probably occurred in recent times, possibly about 2 kya [22]. We calculated the forensic indexes including only the E-M81 subjects and we could observe an even more enhanced clinal pattern (Moroccan DC = 0.87; Libyan DC = 0.96; the values for the Egyptian populations cannot be considered informative because our collection included only four E-M81 chromosomes from this country) (Supplementary Table 12).This haplogroup has been identified in a variety of historically significant populations, including the ancient Phoenicians from Malaka and Selinunte, Medieval Arab communities from Al-Andalus and the Emirate of Sicily, as well as among the indigenous population of the Canary Islands.
| ID | Language | Culture | Country | Location | Date | Study | |||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| I19190 | Semitic | Phoenician | Italy | Selinunte | 700-400BC | Ringbauer at al. 2025 | |||||||||||||||||||||||||||||||||
| I3682 | Semitic | Punico-Roman | Spain | Lucena | 300-400AD | title=Disparate demographic impacts of the Roman Colonization and the Migration Period in the Iberian Peninsula | date=2024-01-01 | biorxiv=10.1101/2024.09.23.614606 | language=en | first1=Pablo | last1=Carrión | first2=Iñigo | last2=Olalde | first3=Juan Manuel | last3=Jiménez-Arenas | first4=Neus | last4=Coromina | first5=David | last5=Vivó | first6=Josep María | last6=Vergès | first7=Ana | last7=Costa | first8=Daniel | last8=Botella | first9=Macarena | last9=Bustamante-Álvarez | first10=Javier | last10=Heras-Mora | first11=Ricardo | last11=Ortega-Ruiz | first12=Celia | last12=Chaves | first13=Maite Iris | last13=García-Collado | first14=Juan Antonio | last14=Quirós-Castillo | first15=Jordi | last15=Roig}} |
| I21367 | Semitic | Punico-Roman | Spain | Malaga | 416-700AD | Carrion et al. 2024 | |||||||||||||||||||||||||||||||||
| GUN012 | Unknown | Guanche | Spain | Tenerife | 593-660 AD | title=Genomic Analyses of Pre-European Conquest Human Remains from the Canary Islands Reveal Close Affinity to Modern North Africans | journal=Current Biology: CB | date=2017-11-06 | issn=1879-0445 | pmid=29107554 | pages=3396–3402.e5 | volume=27 | issue=21 | doi=10.1016/j.cub.2017.09.059 | first1=Ricardo | last1=Rodríguez-Varela | first2=Torsten | last2=Günther | first3=Maja | last3=Krzewińska | first4=Jan | last4=Storå | first5=Thomas H. | last5=Gillingwater | first6=Malcolm | last6=MacCallum | first7=Juan Luis | last7=Arsuaga | first8=Keith | last8=Dobney | first9=Cristina | last9=Valdiosera | first10=Mattias | last10=Jakobsson | first11=Anders | last11=Götherström | first12=Linus | last12=Girdland-Flink | bibcode=2017CBio...27E3396R }} |
| SP7089 | Semitic | Andalusian | France | Narbonne | 637-765 AD | Gleize et al. 2016 | |||||||||||||||||||||||||||||||||
| SP7080 | Semitic | Andalusian | France | Narbonne | 684-761 AD | Gleize et al. 2016 | |||||||||||||||||||||||||||||||||
| 78 | Semitic | Andalusian | Spain | Pamplona | 680-780 AD | de Miguel bánez 2016 | |||||||||||||||||||||||||||||||||
| 107 | Semitic | Andalusian | Spain | Pamplona | 680-780 AD | de Miguel Ibanez 2016 | |||||||||||||||||||||||||||||||||
| GUN011 | Unknown | Guanche | Spain | Tenerife | 704-887 AD | Rodriguez-Varela et al. 2017 | |||||||||||||||||||||||||||||||||
| GOG23 | Semitic | Andalusian | Spain | Vall Uixo | 706-888 AD | Oteo-Garcia et al. 2024 | |||||||||||||||||||||||||||||||||
| CAN02 | Unknown | Guanche | Spain | La Gomera | 774-994 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| ST2933 | Indo-European | Flemish | Belgium | Sint Truiden | 1020-1160 AD | Beneker et al. 2025 | |||||||||||||||||||||||||||||||||
| CAN048 | Unknown | Guanche | Spain | Tenerife | 1028-1162 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| GUN002 | Unknown | Guanche | Spain | Tenerife | 1031-1159 AD | Rodriguez-Varela et al. 2017 | |||||||||||||||||||||||||||||||||
| SGBN3 | Semitic | Andalusian | Italy | Segesta | 1050-1215 AD | Monnereau et al. 2024 | |||||||||||||||||||||||||||||||||
| SGBN1 | Semitic | Andalusian | Italy | Segesta | 1050-1220 AD | Monnereau et al. 2024 | |||||||||||||||||||||||||||||||||
| 112644 | Semitic | Andalusian | Spain | Sagunto | 1100-1300 AD | Olalde et al. 2019 | |||||||||||||||||||||||||||||||||
| 112649 | Semitic | Andalusian | Spain | Sagunto | 1100-1300 AD | Olalde et al. 2019 | |||||||||||||||||||||||||||||||||
| CAN012 | Unknown | Guanche | Spain | Gran Canaria | 1169-1265 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| PT23221 | Semitic | Andalusian | Portugal | Santarem | 1200-1300 AD | Roca-Rada et al. 2024 | |||||||||||||||||||||||||||||||||
| CAN023 | Unknown | Guanche | Spain | Gran Canaria | 1221-1278 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN041 | Unknown | Guanche | Spain | Tenerife | 1228-1297 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN001 | Unknown | Guanche | Spain | Tenerife | 1272-1388 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN030 | Unknown | Guanche | Spain | La Gomera | 1288-1396 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN025 | Unknown | Guanche | Spain | Gran Canaria | 1303-1410 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN043 | Unknown | Guanche | Spain | Gran Canaria | 1322-1437 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN042 | Unknown | Guanche | Spain | Tenerife | 1327-1440 AD | Serrano et al. 2023 | |||||||||||||||||||||||||||||||||
| CAN045 | Unknown | Guanche | Spain | Gran Canaria | 1444-1625 AD | Serrano et al,.2023 | |||||||||||||||||||||||||||||||||
| ELW036 | Indo-European | German | Germany | Ellwangen | 1486-1627 AD | Immel et al. 2021 | |||||||||||||||||||||||||||||||||
| GOG59 | Indo-European | Andalusian | Spain | Vall Uixo | 1501-1600 AD | Oteo-Garcia et al. 2024 | |||||||||||||||||||||||||||||||||
| PT22190 | Indo-European | Portuguese | Spain | Aveiro | 1701-1800 AD | Roca-Rada et al. 2024 |
'''E-PF2431'''
E-PF2431 is a minor subclade of E-L19 mostly found in Europe, with smaller but notable frequencies in the Middle East/North Africa and sub-Saharan Africa. This haplogroup has been identified among Phoenicians from Motya, ancient Romans from Pompeii, and Medieval Arabs.
E-Z830 (E1b1b1b2)
A recently confirmed sub-clade of E-Z827, Z830, includes the confirmed sub-clades of E-M123, E-M293, and E-V42, and is a sibling clade to E-L19. Currently, the E-M35 phylogeny project recognizes four distinct clusters of Z830* carriers, two of which are exclusively Jewish in origin. The remaining two are significantly smaller, and include scattered individuals in Germany, Spain, Latin America, Egypt, and Ethiopia.
E-M123
Main article: Haplogroup E-M123 (Y-DNA)
E-M123 is mostly known for its major subclade E-M34, which dominates this clade.
E-V1515
A new clade (E-V1515) was defined by Trombetta et al. 2015, which originated about 12 kya (95% CI 8.6-16.4) in eastern Africa where it is currently mainly distributed. This clade includes all the sub-Saharan haplogroups (E-V42, E-M293, E-V92, E-V6) reported as E-M35 basal clades in a previous phylogeny.
We observed the highest frequency and diversity of this haplogroup in the northern part of the Horn of Africa (present day Eritrea and northern Ethiopia), where the majority of the deepest E-V1515 subhaplogroups and paragroups were found. In the southern part of the Horn (southern Ethiopia, Somalia and northern Kenya), haplogroup E-V1515 is almost exclusively represented by the recent (3.5 ka; 95% CI: 1.7–5.9 ka) subhaplogroup E-V1486. Further south, in southern Kenya and southern Africa, a single E-V1486 terminal clade, known as E-M293 (Henn et al. 2008), was found (fig. 3). This phylogeographic pattern is strongly suggestive of human movements from the northern part of the Horn to the Ethiopian/Kenyan borders between 12 ka (the coalescence of E-V1515) and 3.5 ka (the coalescence of E-V1486), and from here toward southern Africa across the equatorial belt in more recent times.
Multiple instances of commercially observed E-V1515 have also been detected in Arabia.
E-M293
E-M293 is a subclade of E-V1515. It was identified by ISOGG as the second clade within E-Z830. It was discovered before E-Z830 and is associated with the spread of pastoralism from Eastern Africa by South Cushites into Southern Africa. So far high levels have been found in specific ethnic groups in Tanzania and Southern Africa. Highest were the Datog (43%), Khwe (Kxoe) (31%), Burunge (28%), and Sandawe (24%). Two Bantu-speaking Kenyan males were found with the M293 mutation. Other E-M215 subclades are rare in Southern Africa. The authors state...
Without information about M293 in the Maasai, Hema, and other populations in Kenya, Sudan, and Ethiopia, we cannot pinpoint the precise geographic source of M293 with greater confidence. However, the available evidence points to present-day Tanzania as an early and important geographic locus of M293 evolution.
They also say that "M293 is only found in sub-Saharan Africa, indicating a separate phylogenetic history for M35.1 * (former) samples further north". E-P72. This is a subclade of E-M293.
E-V42
E-V42 was discovered in two Ethiopian Jews. It was suggested that it may be restricted to the region around Ethiopia. However, further testing by commercial DNA testing companies confirmed positive results for this subclade in Arabia as well.
E-V6
The E-V6 subclade of E-V1515 is defined by V6 and has been identified a significant presence of these lineages in Ethiopia, and also some in the neighboring Somali population. Among the Ethiopian and Somali samples, the highest were 14.7% among the Ethiopian Amhara, and 16.7% among the Ethiopian Wolayta.
E-V92
E-V92 was discovered in two Ethiopian Amhara. Like E-V6 and E-V42 it possibly only exists in the area of Ethiopia.
Phylogenetics
Phylogenetic History
Main article: Conversion table for Y chromosome haplogroups
Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
| YCC 2002/2008 (Shorthand) | (α) | (β) | (γ) |
|---|---|---|---|
| (δ) | (ε) | (ζ) | (η) |
| E-P29 | 21 | III | 3A |
| E-M33 | 21 | III | 3A |
| E-M44 | 21 | III | 3A |
| E-M75 | 21 | III | 3A |
| E-M54 | 21 | III | 3A |
| E-P2 | 25 | III | 4 |
| E-M2 | 8 | III | 5 |
| E-M58 | 8 | III | 5 |
| E-M116.2 | 8 | III | 5 |
| E-M149 | 8 | III | 5 |
| E-M154 | 8 | III | 5 |
| E-M155 | 8 | III | 5 |
| E-M10 | 8 | III | 5 |
| E-M35 | 25 | III | 4 |
| E-M78 | 25 | III | 4 |
| E-M148 | 25 | III | 4 |
| E-M81 | 25 | III | 4 |
| E-M107 | 25 | III | 4 |
| E-M165 | 25 | III | 4 |
| E-M123 | 25 | III | 4 |
| E-M34 | 25 | III | 4 |
| E-M136 | 25 | III | 4 |
Original Research Publications
The following research teams per their publications were represented in the creation of the YCC Tree.
- α
- β
- γ
- δ
- ε
- ζ
- η
References
References
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