chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186061976660619767TG27GENICheterozygous809945159
186062046560620466TC50GENIChomozygous809945160
186062060360620604TC51GENIChomozygous809945161
186062134660621347GA48GENIChomozygous809945162
186062329660623297TC45GENICheterozygous809945163
186062330860623309CT41GENICheterozygous809945164
186062424960624250GA56GENIChomozygous809945165
186062580060625801TC34GENIChomozygous809945166
186062624260626243AT46GENIChomozygous809945167
186062663260626633TC45GENIChomozygous809945168
186062687160626872CT49GENIChomozygous809945169
186062748460627485TC67GENIChomozygous809945170
186062880060628801AG44GENIChomozygous809945171
186063125160631252CT50GENIChomozygous809945172
186063150960631510GA59GENIChomozygous809945173