chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228477949228477950TC14GENIChomozygous61107089
1228477987228477988GC16GENICpossibly homozygous61107090
1228478166228478167CT15GENIChomozygous61107091
1228478841228478842TC18GENIChomozygous61107092
1228479873228479874TG17GENIChomozygous61107096
1228480563228480564GA28GENIChomozygous61107097
1228480887228480888GC3GENICheterozygous61107098
1228481672228481673CT3GENIChomozygous61107099