Table 1 Summary of genotyping data against the Reconstructed Sapiens Reference Sequence (RSRS).

From: Neolithic mitochondrial haplogroup H genomes and the genetic origins of Europeans

Culture/age

Individual

Hg *

Hg H sequence variants compared with RSRS

LBK (5450–4775 BC)

HAL36

H23

C10211T

 

HAL11

H

T16093C, G16129A!

 

HAL32

H26

T11152C

 

HAL39

H1e

G3010A, G5460A

 

DEB9

H88

A8596G

 

DEB21

H1j

G3010A, T4733C

 

KAR6a

H1bz

G1719A, G3010A, C14380T

 

KAR11b

H

T152C!

 

KAR16a

H46b

C2772T, A11893G

Rössen (4625–4475/4250 BC)

OSH2

H89

A6932G, C8068T, T12696C

 

OSH3

H1

G3010A

 

OSH1

H16

T152C!, C10394T

 

OSH7

H5b

C456T, G5471A, T16304C, C16519T

Schöningen (4100–3950 BC)

SALZ18a

H10i

C13503T, T14470a, T16093C

 

SALZ21b

H1e7

T1766C, G3010A, G5460A

Baalberge (3950–3400 BC)

ESP30

H1e1a5

G3010A, G5460A, (C5960T), A8512G, G8865A, C14902T

 

HQU4

H7d5

A4793G, C15409T, G16388A

Salzmünde (3400–3100/3025 BC)

SALZ57a

H3

T152C!, T6776C

 

SALZ77a

H3

T6776C

Corded Ware (2800–2200/2050 BC)

ESP15

H6a1a

T239C, G3915A, A4727G, G9380A, T11253C, T16362C, A16482G, C16519T

 

BZH6

H1_TBD

G3010A, A8149G, A9377G, T9467C, A13671G, T14319C, T16189C!

Bell Beaker

BZH4

H1e7

G3010A, G5460A, A15220G, A15401G, A16293G

(2500–2200/2050 BC)

ROT6

H5a3

C456T, G513A, T4336C, G15884A, T16304C, C16519T

 

ALB1

H3b

A2581G, T6776C

 

ROT1

H3ao2

C4577T, T6776C, C16256T

 

ROT2

H5a3

C456T, G513A, T4336C, G15884A, T16304C, C16519T

 

QUEXII1

H4a1

C3992T, A4024G, T5004C, G9123A, C14365T, A14582G, C16519T

 

QUEXII2

H4a1

C3992T, A4024G, T5004C, G9123A, C14365T, A14582G, C16519T

 

QLB26a

H1

G3010A

 

QUEXII3

H13a1a2c

C2259T, A4745G, G9025A, A13542G, C13680T, C14872T, C16519T

 

QLB28b

H1

G3010A

Unetice (2200–1575 BC)

BZH1

H11a

T195C!, T961g, T8448C, (G13759A), A16293G, T16311C!, C16519T

 

BZH8

H2a1a3

G951A, G1438A, G4769A, C6173T, T13095C, A16240t, C16354T, C16519T

 

BZH14

H82a

T195C!, A16220G

 

EUL41a

H4a1a1a5

A73G!, C3992T, A4024G, T5004C, G8269A, G9123A, A10044G, C13545T, C14365T, A14582G, C16519T

 

EUL57B

H3

T152C!, T6776C

 

QUEVIII4

H7h

A4793G, G16213A

Nuragic Bronze Age (1624 BC)

H1aw1

G3010A, A8701G!, C15912T

Iron Age (500 BC)

H90

C5435T, T8911C, T10237C, T15109C

  1. Abbreviation: SNP, single-nucletide polymorphism.
  2. Sub-haplogroup defining diagnostic SNPs are shown in bold and ‘private’/as-yet-unknown sequence variants in regular print.
  3. *Haplogroup H designations based on the http://www.phylotree.org mtDNA tree Build 14 (5 April 2012)19,20.