chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186061976660619767TG21GENICpossibly homozygous814389605
186062046560620466TC25GENIChomozygous814389606
186062060360620604TC33GENIChomozygous814389607
186062134660621347GA37GENIChomozygous814389608
186062329660623297TC42GENICheterozygous814389609
186062424960624250GA26GENIChomozygous814389610
186062580060625801TC29GENIChomozygous814389611
186062624260626243AT43GENIChomozygous814389612
186062663260626633TC19GENIChomozygous814389613
186062687160626872CT33GENIChomozygous814389614
186062748460627485TC24GENIChomozygous814389615
186062880060628801AG29GENIChomozygous814389616
186063125160631252CT41GENIChomozygous814389617
186063150960631510GA21GENIChomozygous814389618