chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT55GENIChomozygous135505436
11286211012862111AG37GENIChomozygous135505437
11286224612862247TC48GENIChomozygous135505438
11286231612862317TC43GENIChomozygous135505439
11286274412862745GT52GENIChomozygous135505440
11286355912863560TG53GENICpossibly homozygous135505441
11286364212863643TA47GENIChomozygous135505442
11286367612863677CT34GENIChomozygous135505443
11286372912863729GTGT20GENIChomozygous135395483
11286363712863641GTGC47GENIChomozygous135395481
11286366512863667GC41GENIChomozygous135395482
11286375312863753GTGTGC10GENIChomozygous135395484
11286379712863799GC9GENIChomozygous135395485
11286381512863817GC14GENIChomozygous135395486
11286382312863829GTGTGT13GENIChomozygous135395487
11286384112863843GC18GENIChomozygous135395488
11286384412863845CT19GENIChomozygous135505444
11286411612864117GC30GENIChomozygous135505445
11286621612866217GA57GENIChomozygous135505446
11286722812867229AG50GENIChomozygous135505447
11286723112867232AG48GENIChomozygous135505448
11286788312867884TC39GENIChomozygous135505449
11286801812868019AC45GENIChomozygous135505450
11286873212868732AAAT29GENIChomozygous135395489
11286876512868767GT29GENIChomozygous135395490
11286899912869000G16GENIChomozygous135395491
11286900312869009TGTGTA16GENIChomozygous135395492
11286901812869024TGGTGT14GENIChomozygous135395493
11286962312869624AG40GENIChomozygous135505451
11287030512870306AG39GENIChomozygous135505452
11287144212871443TC49GENIChomozygous135505453
11287245512872456TA59GENIChomozygous135505454