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. 2016 Jun 1;11(6):e0155508. doi: 10.1371/journal.pone.0155508

Table 1. Haplogroup determination and mtDNA genomic coverage for Huaca Pucllana samples.

# Sample number Culture Haplogroup Coverage of the mitogenome Average coverage depth per position (min–max) StdDev Additional mutations from the hg node GenBank accession number
1 10791 Lima A2 100% 122.7 (1–59) 13.5 C64T, 356.1C, T1189C, A5222G, T15289C, G16129A!, T16189C! KU523266
2 10814 Lima B2 100% 164.6 (9–186) 14.3 T2857C, T5082C, T5277C, A15924G, T16330C KU523287
3 10802 Lima B2 100% 63.4 (1–105) 14.4 C16168T KU523286
4 10789 Lima B2b 100% 100.2 (5–141) 15.1 G6261A, G9055A, A12972G, A14053G KU523283
5 10817 Lima C1b 100% 132.2 (5–169) 16.4 A9468G, C12535T, T15313C, A16166C, T16223C KU523324
6 10820 Lima C1b 100% 84.6 (1–135) 15.8 A9468G, C12535T, T15313C, A16166C, T16223C KU523325
7 10806 Lima C1c 100% 73.4 (1–117) 17.1 T152C!, 7472d, T8450C, C12774T, T16172C, T16297C KU523322
8 10811 Lima D4/ Pre-D1/D1 99. 99% 50.4 (0–97) 14.9 G143A, T2092C!, A6113G, T16189C!, G16274A, C16365T KU523345
9 10821 Lima B2 100% 98.2 (1–149) 19.9 T146C!,T3786C, A8170G, G15777A KU523288
10 10774 Wari A2 100% 67.7 (1–115) 18.1 C64T, A675G, A3354, T6911C, A13966G, C14800A, G16145A KU523264
11 10754 Wari B2b 100% 48.8 (1–99) 17 A243G, C4013T, G8994A, G11016A, G12127A, A14059G, G16438A KU523282
12 10734 Wari C1b 100% 59.8 (1–104) 17.3 C12535T, T15313C, A16166C, G16244T KU523317
13 10763 Wari C1b 99.90% 20.7 (0–55) 9 C12535T, T15313C KU523318
14 10771 Wari C1b 98.80% 18.2 (0–50) 8.2 A9468G, C12535T, T15313C, A16166C KU523320
15 10773 Wari C1b 100% 78.0 (0–119) 15.2 T8380C, T13281C, A13710C, A15244G, C15315T, A16207G KU523321
16 10778 Wari A2 97.60% 20.5 (0–100) 15.6 C64T, T1189C, T3786C, A5222G, C5765T, A7673G, T8738C, T15289C, C16221T, G12127A KU523265
17 10765 Wari C1b 99.80% 105.2 (0–340) 62.5 C12535T, T15313C, A16166C, G16244T KU523319
18 10750 Wari B2b 98.70% 22.3 (0–97) 16.7 T152C!, G1797A, A9377G, G12127A, A14053G, C14428T KU523281
19 10742 Wari B2b 100% 84.3 (0–248) 40.2 A178G, A6779G, A10420G, C16278T! C16295T KU523280
20 10713 Ychsma B2 100% 109.5 (2–163) 21.9 573.1C, A5186G, C5375T, C5895T, G15884A KU523276
21 10729 Ychsma B2 100% 101.6 (0–171) 24.8 T152C!, A2880G, C7786T, C13934T, A16051G, C16360T KU523279
22 10720 Ychsma B2b 100% 171.6 (19–191) 14.4 G6261A, G9055A, A14053G, C15647T KU523277
23 10726 Ychsma B2b 99.96% 38.5 (0–88) 14.7 G143A, T9078C, G10530A, A14053G, G16390A KU523278
24 10709 Ychsma C1b 100% 146.6 (0–176) 18.1 C12535T, T15313C KU523313
25 10717 Ychsma C1b 100% 175 (18–191) 11.9 C150T, T152C!, C12535T, T15313C, C16292T KU523314
26 10725 Ychsma C1b 100% 177.9 (0–192) 16.6 C12535T, T15313C KU523315
27 10731 Ychsma C1b 100% 182 (0–193) 17.7 A636G, C3442T, C4496T, G5821A, A5894C, G16000A, T16362C KU523316
28 10722 Ychsma D1 100% 140.8 (0–181) 21 T11365C, G11906A, T12481C, C12557T, A14665G KU523342
29 10732 Ychsma D4/ Pre-D1/D1 100% 146.6 (0–180) 18.1 G143A, T2092C!, A6113G, T16189C!, G16274A, C16365T KU523343
30 10730 Ychsma B2b 99.80% 46.0 (0–102) 20.2 T131C, C4013T, G13708A, T14634C, T15784C KU523275
31 10805 Ychsma D1 100% 159.5 (7–186) 13.1 T11365C, G11906A, T12481C, C12557T, A14665G KU523344
32 10810 Ychsma C1d 99.90% 90.3 (0–166) 39.4 A14122G KU523323
33 10794 Ychsma B2 99.60% 16.8 (0–54) 8.9 G8290A, A16066G KU523284
34 10800 Ychsma B2b 100% 127.6 (4–166) 17.2 T131C,C4013T, G13708A, T14634C, C14873A, T15784C KU523285

Additional variants from the sub-haplogroup nodes compared to RSRS [30]. We generally follow the nomenclature of Phylotree.org [31], in describing variants: Reversions (back mutations) to an ancestral state are indicated with an exclamation mark (!), while 7472d and 356.1C denotes a deletion or insertion at the given nucleotide position, respectively.