chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1215044118215044119AT16GENIChomozygous108533401
1215048235215048236TA20GENIChomozygous109192092
1215048482215048483CT28GENIChomozygous109192094
1215048560215048561CT12GENIChomozygous109192096
1215055901215055902GA21GENIChomozygous109192100
1215058632215058633AG23GENIChomozygous109192102
1215066872215066873AG18GENIChomozygous108533419
1215066971215066972AG18GENIChomozygous108533421
1215069828215069829GT9GENIChomozygous120475845
1215070956215070957CT21GENIChomozygous120475846
1215071082215071083GT12GENIChomozygous108533436
1215071121215071122GT17GENIChomozygous120511849
1215072038215072039AG22GENIChomozygous108533442
1215074866215074867GA19GENIChomozygous109192104
1215075927215075928GT23GENIChomozygous108533443
1215077079215077080TC18GENIChomozygous108533444
1215077900215077901AG14GENIChomozygous109192106
1215078673215078674CT18GENIChomozygous109192108
1215079568215079569GC28GENIChomozygous109192110
1215098358215098359GC14GENIChomozygous109192112
1215099469215099470CT16GENIChomozygous109192114
1215101155215101156CT23GENIChomozygous109192120
1215102908215102909CT24GENIChomozygous108533470
1215103130215103131TC23GENIChomozygous108533471