chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10105765631105765632A22GENIChomozygous138703493
10105765806105765807GC32GENIChomozygous138868134
10105765870105765870TA33GENIChomozygous138703494
10105766258105766259AG18GENIChomozygous138868135
10105766479105766480GT24GENIChomozygous138868136
10105766511105766512TC21GENIChomozygous138868137
10105766673105766674GT25GENIChomozygous138868138
10105766769105766770CT25GENIChomozygous138868139
10105767784105767785AG20GENIChomozygous138868140
10105768745105768746TC16GENIChomozygous138868141
10105772851105772852CT30GENIChomozygous138868142
10105774488105774489AG14GENIChomozygous138868143
10105774496105774496G13GENIChomozygous138703495