chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT64GENIChomozygous135505436
11286211012862111AG38GENIChomozygous135505437
11286224612862247TC47GENIChomozygous135505438
11286231612862317TC39GENIChomozygous135505439
11286274412862745GT56GENIChomozygous135505440
11286355912863560TG53GENIChomozygous135505441
11286363712863641GTGC39GENICpossibly homozygous135395481
11286364212863643TA39GENICpossibly homozygous135505442
11286366512863667GC39GENIChomozygous135395482
11286367612863677CT38GENIChomozygous135505443
11286372912863729GTGT19GENIChomozygous135395483
11286375312863753GTGTGC11GENIChomozygous135395484
11286379712863799GC9GENIChomozygous135395485
11286381512863817GC9GENIChomozygous135395486
11286382312863829GTGTGT10GENIChomozygous135395487
11286384112863843GC14GENIChomozygous135395488
11286384412863845CT14GENIChomozygous135505444
11286411612864117GC40GENIChomozygous135505445
11286621612866217GA66GENIChomozygous135505446
11286722812867229AG58GENIChomozygous135505447
11286723112867232AG55GENIChomozygous135505448
11286788312867884TC53GENIChomozygous135505449
11286801812868019AC66GENICpossibly homozygous135505450
11286873212868732AAAT27GENIChomozygous135395489
11286901812869024TGGTGT17GENIChomozygous135395493
11286876512868767GT27GENIChomozygous135395490
11286899912869000G16GENIChomozygous135395491
11286900312869009TGTGTA17GENIChomozygous135395492
11286962312869624AG53GENIChomozygous135505451
11287030512870306AG47GENIChomozygous135505452
11287144212871443TC46GENIChomozygous135505453
11287245512872456TA70GENIChomozygous135505454