chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT25GENIChomozygous135505436
11286211012862111AG12GENIChomozygous135505437
11286224612862247TC17GENIChomozygous135505438
11286231612862317TC16GENIChomozygous135505439
11286274412862745GT23GENIChomozygous135505440
11286355912863560TG19GENIChomozygous135505441
11286364212863643TA19GENICpossibly homozygous135505442
11286367612863677CT17GENICpossibly homozygous135505443
11286379712863799GC5GENIChomozygous135395485
11286363712863641GTGC19GENICpossibly homozygous135395481
11286366512863667GC18GENICpossibly homozygous135395482
11286372912863729GTGT11GENIChomozygous135395483
11286375312863753GTGTGC5GENIChomozygous135395484
11286381512863817GC6GENIChomozygous135395486
11286382312863829GTGTGT6GENIChomozygous135395487
11286384112863843GC6GENIChomozygous135395488
11286384412863845CT6GENIChomozygous135505444
11286411612864117GC23GENIChomozygous135505445
11286621612866217GA17GENIChomozygous135505446
11286722812867229AG34GENIChomozygous135505447
11286723112867232AG35GENIChomozygous135505448
11286788312867884TC28GENIChomozygous135505449
11286801812868019AC24GENIChomozygous135505450
11286873212868732AAAT11GENIChomozygous135395489
11286876512868767GT22GENIChomozygous135395490
11286962312869624AG25GENIChomozygous135505451
11287030512870306AG19GENIChomozygous135505452
11287144212871443TC22GENIChomozygous135505453
11287245512872456TA20GENIChomozygous135505454