chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6103944473103944474GC58GENICpossibly homozygous114929253
6103944990103944991CT7GENIChomozygous126361122
6103945569103945570TC13GENIChomozygous126451039
6103945660103945661AT18GENIChomozygous126361124
6103945686103945687AT11GENICheterozygous126361126
6103947214103947215TC5GENIChomozygous114929418