chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11285831512858316CT21GENIChomozygous135505436
11286211012862111AG23GENIChomozygous135505437
11286224612862247TC18GENIChomozygous135505438
11286231612862317TC20GENIChomozygous135505439
11286274412862745GT30GENIChomozygous135505440
11286355912863560TG16GENIChomozygous135505441
11286364212863643TA19GENIChomozygous135505442
11286367612863677CT20GENIChomozygous135505443
11286372912863729GTGT13GENIChomozygous135395483
11286363712863641GTGC18GENIChomozygous135395481
11286366512863667GC20GENIChomozygous135395482
11286375312863753GTGTGC9GENIChomozygous135395484
11286379712863799GC5GENIChomozygous135395485
11286381512863817GC7GENIChomozygous135395486
11286382312863829GTGTGT8GENIChomozygous135395487
11286384112863843GC9GENIChomozygous135395488
11286384412863845CT9GENIChomozygous135505444
11286411612864117GC20GENIChomozygous135505445
11286621612866217GA27GENIChomozygous135505446
11286722812867229AG26GENIChomozygous135505447
11286723112867232AG26GENIChomozygous135505448
11286788312867884TC17GENIChomozygous135505449
11286801812868019AC20GENIChomozygous135505450
11286873212868732AAAT16GENIChomozygous135395489
11286876512868767GT21GENIChomozygous135395490
11286899912869000G14GENIChomozygous135395491
11286900312869009TGTGTA14GENIChomozygous135395492
11286901812869024TGGTGT14GENIChomozygous135395493
11286962312869624AG29GENIChomozygous135505451
11287030512870306AG26GENIChomozygous135505452
11287144212871443TC24GENIChomozygous135505453
11287245512872456TA18GENIChomozygous135505454