chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227409520227409521AC29GENIChomozygous120512364
1227409521227409522GA28GENIChomozygous120512365
1227409551227409552CA26GENIChomozygous108999148
1227410130227410131TC26GENIChomozygous108999149
1227410145227410146TC30GENIChomozygous108999150
1227410406227410407AC28GENIChomozygous108999151
1227411765227411766AG22GENIChomozygous108999152
1227411975227411976AC16GENIChomozygous108999153
1227412211227412212TC22GENIChomozygous108999154
1227412235227412236AG18GENIChomozygous108999155
1227413022227413023CT24GENIChomozygous109199062
1227413211227413212GC16GENIChomozygous108999156
1227414517227414518GA9GENIChomozygous108999166
1227414676227414677CA5GENIChomozygous108999167