chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16578187465781875GC50GENIChomozygous109487270
16578203965782040TC40GENIChomozygous109487271
16578512765785128CA17GENIChomozygous120866588
16578532865785329TC16GENIChomozygous109487275
16578547465785475CT33GENIChomozygous120866589
16578551065785511TG37GENIChomozygous120866590
16578858165788582CT23GENIChomozygous120866593
16578949465789495TG12GENIChomozygous109487277
16579052165790522AG26GENIChomozygous120866594
16579090865790909AT24GENIChomozygous120866595
16579153165791532AG45GENIChomozygous120866596
16579175965791760TC11GENIChomozygous120866597
16579332765793328TC31GENIChomozygous109487279
16579359365793594CT13GENIChomozygous120866598
16579394765793948CA48GENIChomozygous109487280
16579498865794989GT35GENIChomozygous120866599
16579503265795033CT35GENIChomozygous120866600
16579505265795053TC26GENIChomozygous109487281
16579655065796551AG21GENIChomozygous120866602
16579707965797080AG39GENIChomozygous109487282
16579727365797274CT22GENIChomozygous120775033
16579776565797766AG8GENIChomozygous109487284
16579802065798021CT22GENIChomozygous109487286
16579815965798160CT29GENIChomozygous120866603
16579816665798167GA31GENIChomozygous120866604
16579816865798169CT28GENIChomozygous120866605
16579846465798465CT13GENIChomozygous109487287
16579865765798658CA13GENIChomozygous109487288
16579917565799176GT17GENIChomozygous109487289
16579680665796807AG49GENIChomozygous108860573