chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141763972417639725TC17GENIChomozygous967845607
141764052517640526TC24GENIChomozygous967845608
141764261817642619CT20GENIChomozygous967845609
141764265617642657CA21GENIChomozygous967845610
141764342217643423GC21GENIChomozygous967845611
141764352417643525CT17GENIChomozygous967845612
141764359417643595CA17GENICpossibly homozygous967845613
141764416617644167GT26GENIChomozygous967845614
141764622417646225CT22GENIChomozygous967845615
141764869017648691GC12GENIChomozygous967845616
141764987017649871CA15GENIChomozygous967845617
141765004317650044CT23GENIChomozygous967845618
141765048617650487CT23GENIChomozygous967845619
141765054617650547TC23GENIChomozygous967845620
141765054917650550CT23GENIChomozygous967845621
141765055317650554GA26GENIChomozygous967845622
141765061417650615CT25GENIChomozygous967845623
141765064217650643AT23GENIChomozygous967845624
141765064417650645AT24GENIChomozygous967845625
141765067217650673TG22GENIChomozygous967845626
141765072117650722AG19GENIChomozygous967845627
141765115717651158AT7GENIChomozygous967845628
141765141217651413AT17GENIChomozygous967845629
141765144717651448TG17GENIChomozygous967845630
141765161617651617AG20GENIChomozygous967845631
141765171117651712GC25GENIChomozygous967845632
141765171817651719GA21GENIChomozygous967845633
141765172617651727GT23GENIChomozygous967845634
141765179617651797GA15GENIChomozygous967845635
141765416017654161GA18GENIChomozygous967845636
141765416217654163AG18GENIChomozygous967845637
141765581617655817TC27GENIChomozygous967845638
141765645617656457TC28GENIChomozygous967845639
141765649817656499CT23GENICpossibly homozygous967845640
141765685017656851AG23GENIChomozygous967845641