chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT24GENIChomozygous135505436
11286211012862111AG15GENIChomozygous135505437
11286224612862247TC15GENIChomozygous135505438
11286231612862317TC16GENIChomozygous135505439
11286274412862745GT23GENIChomozygous135505440
11286355912863560TG24GENICpossibly homozygous135505441
11286364212863643TA16GENIChomozygous135505442
11286367612863677CT12GENIChomozygous135505443
11286375312863753GTGTGC5GENIChomozygous135395484
11286363712863641GTGC16GENIChomozygous135395481
11286366512863667GC14GENIChomozygous135395482
11286372912863729GTGT7GENIChomozygous135395483
11286379712863799GC9GENIChomozygous135395485
11286381512863817GC12GENIChomozygous135395486
11286382312863829GTGTGT15GENIChomozygous135395487
11286384112863843GC16GENIChomozygous135395488
11286384412863845CT16GENIChomozygous135505444
11286411612864117GC16GENIChomozygous135505445
11286621612866217GA15GENIChomozygous135505446
11286722812867229AG13GENIChomozygous135505447
11286723112867232AG12GENIChomozygous135505448
11286788312867884TC9GENIChomozygous135505449
11286801812868019AC14GENIChomozygous135505450
11286873212868732AAAT11GENIChomozygous135395489
11286876512868767GT18GENIChomozygous135395490
11286899912869000G11GENIChomozygous135395491
11286900312869009TGTGTA11GENIChomozygous135395492
11286901812869024TGGTGT11GENIChomozygous135395493
11286962312869624AG18GENIChomozygous135505451
11287030512870306AG20GENIChomozygous135505452
11287144212871443TC15GENIChomozygous135505453
11287245512872456TA28GENIChomozygous135505454