chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT64GENIChomozygous135505436
11286211012862111AG49GENIChomozygous135505437
11286224612862247TC58GENIChomozygous135505438
11286231612862317TC48GENIChomozygous135505439
11286274412862745GT61GENIChomozygous135505440
11286355912863560TG49GENIChomozygous135505441
11286364212863643TA33GENIChomozygous135505442
11286367612863677CT26GENIChomozygous135505443
11286379712863799GC16GENIChomozygous135395485
11286363712863641GTGC31GENIChomozygous135395481
11286366512863667GC30GENICpossibly homozygous135395482
11286372912863729GTGT15GENIChomozygous135395483
11286375312863753GTGTGC8GENIChomozygous135395484
11286381512863817GC18GENIChomozygous135395486
11286382312863829GTGTGT19GENIChomozygous135395487
11286384112863843GC21GENICpossibly homozygous135395488
11286384412863845CT21GENICpossibly homozygous135505444
11286411612864117GC44GENIChomozygous135505445
11286621612866217GA55GENIChomozygous135505446
11286722812867229AG59GENICpossibly homozygous135505447
11286723112867232AG59GENICpossibly homozygous135505448
11286788312867884TC52GENIChomozygous135505449
11286801812868019AC47GENIChomozygous135505450
11286873212868732AAAT27GENIChomozygous135395489
11286876512868767GT29GENIChomozygous135395490
11286899912869000G12GENIChomozygous135395491
11286900312869009TGTGTA11GENIChomozygous135395492
11286901812869024TGGTGT11GENIChomozygous135395493
11286962312869624AG45GENIChomozygous135505451
11287030512870306AG71GENIChomozygous135505452
11287144212871443TC58GENIChomozygous135505453
11287245512872456TA60GENIChomozygous135505454