chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122217886922178870CT32GENIChomozygous115366487
122217907522179075CC27GENIChomozygous128970348
122217914122179141TC8GENIChomozygous128970349
122217960322179604CA54GENIChomozygous115280581
122217960722179608GA52GENIChomozygous115280583
122217961822179619TC54GENIChomozygous115280585
122218047422180474CCCAAC39GENIChomozygous128970350
122218089622180897TC40GENIChomozygous115280587
122218202922182030GC55GENIChomozygous115280589
122218217822182179G51GENIChomozygous128970351
122218293522182936GA38GENIChomozygous115280591
122218297522182976TC41GENIChomozygous115280593
122218547222185473TC43GENIChomozygous115280595
122217933522179335C8GENIChomozygous130042072
122218553222185533TC53GENICpossibly homozygous115664501
122218587822185879TG34GENIChomozygous115664503
122218657522186576GA42GENIChomozygous115664505
122218702422187025AG33GENIChomozygous115664507
122218754922187550TC57GENIChomozygous115280599
122218758622187587CG53GENIChomozygous115664510
122218760522187606GA49GENIChomozygous115280601
122218761422187615AG47GENIChomozygous115664512
122218813022188131TC25GENIChomozygous115280605
122218828022188281G15GENIChomozygous128970353
122218834122188342CG24GENIChomozygous123663193
122218846022188461CT36GENICpossibly homozygous123663194
122218859122188596TTCTT2GENIChomozygous128970354
122219027522190276GA41GENIChomozygous115664514
122219032022190321GA46GENIChomozygous115664516
122219107722191078T35GENICpossibly homozygous133496140
122219184222191843C37GENIChomozygous128970359
122219293922192940CG52GENIChomozygous115280621
122219054222190543GA35GENIChomozygous115664518
122219058722190588AC43GENIChomozygous115664520
122219087222190873AT46GENIChomozygous115280609
122219140422191405AG46GENIChomozygous115664522
122219156422191565TA36GENIChomozygous115280613
122219176622191767TC50GENIChomozygous115664524
122219233622192337TC48GENIChomozygous115280619
122219307322193074AG46GENIChomozygous115664526
122219342722193428AT47GENIChomozygous115664528