chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75093032350930324TC17GENIChomozygous53918512
75093104250931043GA44GENICheterozygous54735788
75093136150931362CT40GENICheterozygous53918513
75093145550931456CA63GENICheterozygous53918514
75093179250931793AG31GENICpossibly homozygous53918515
75093198450931985AG30GENICpossibly homozygous53918516
75093222150932222GA25GENIChomozygous53918517
75093269950932700AC87GENICheterozygous54735790
75093273750932738TC45GENICheterozygous54735792
75093276350932764GC18GENICheterozygous53918518
75093276950932770TG12GENICheterozygous53918519
75093290750932908TC32GENICheterozygous53918520
75093328950933290TC23GENIChomozygous53918521
75093360350933604CT21GENICheterozygous53918525
75093367750933678TC60GENICheterozygous53918526
75093393350933934TC27GENIChomozygous53918527
75093405650934057GA20GENICheterozygous53918528
75093438750934388CA74GENICheterozygous54386917
75093465050934651AC42GENICheterozygous53918529
75093474050934741GA50GENICheterozygous53918530
75093500950935010CT36GENICheterozygous53918531
75093507950935080GT2GENIChomozygous54735794
75093529850935299GA31GENICheterozygous54195390
75093527850935279AG40GENICheterozygous54195389
75093510750935108AG8GENICheterozygous54651064
75093513050935131TA10GENICheterozygous54651066
75093706250937063GT25GENICheterozygous54195391
75093707150937072CT21GENICheterozygous53918533
75093707250937073AG21GENICheterozygous53918534
75093733450937335GT30GENICpossibly homozygous53918535
75093773950937740GC15GENIChomozygous53918536
75093774050937741GT15GENIChomozygous53918537
75093774550937746GGC13GENIChomozygous53918538
75093778950937790GA19GENIChomozygous53918539
75093784050937841TG17GENIChomozygous53918540
75093784450937845A-15GENIChomozygous53918541
75093789950937903TAAT----17GENIChomozygous53918542
75093819050938191CT10GENIChomozygous53918543
75093862650938627GT18GENIChomozygous53918544
75094110250941103GC20GENIChomozygous53918545