chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256956413256956414T-8GENIChomozygous62277204
1256956879256956880AT7GENIChomozygous62851269
1256957310256957311T-9GENIChomozygous61170599
1256960645256960646CT10GENICheterozygous61170608
1256961777256961778CT17GENIChomozygous61170612
1256962109256962110CT23GENIChomozygous61170613
1256962304256962305TC22GENIChomozygous61170614
1256962616256962617TC18GENIChomozygous61170615
1256962712256962713AT15GENIChomozygous61170616
1256963164256963165A-11GENIChomozygous61170617
1256964314256964315TC16GENIChomozygous61170618
1256965321256965322TG25GENIChomozygous61170619
1256965815256965816GGTA23GENIChomozygous61170620
1256967624256967625TC25GENIChomozygous61170622
1256968523256968524AC20GENIChomozygous61170623
1256970483256970487ATAT----12GENIChomozygous62277205
1256970503256970504AG12GENIChomozygous61170625
1256971334256971335TC17GENIChomozygous61170626
1256974099256974100CT7GENIChomozygous62851270
1256974665256974666TTAA14GENICheterozygous61170627
1256975041256975042GA10GENICheterozygous61170632
1256975796256975797CG15GENIChomozygous61170634
1256976102256976103GA10GENIChomozygous61170635
1256976610256976611TG13GENIChomozygous61170636
1256982288256982289GC21GENIChomozygous61170639
1256984211256984212T-21GENIChomozygous61170640
1256986554256986555GA25GENICpossibly homozygous61170641
1256987775256987776GC13GENIChomozygous61170642
1256989545256989546T-19GENIChomozygous61170643
1256990113256990114GA22GENIChomozygous61170644
1256991006256991007GA20GENIChomozygous61170645
1256991396256991397AG16GENIChomozygous61170646
1256991476256991477TC14GENIChomozygous61170647
1256994275256994276CA15GENIChomozygous61170650
1256994283256994284CA15GENIChomozygous61170651