chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
186965179869651799AG14GENIChomozygous46746089
186965207669652077TC18GENIChomozygous46746090
186965209369652094TC23GENIChomozygous46746091
186965408969654090CT9GENIChomozygous46746093
186965504069655041AG20GENIChomozygous46746095
186965518369655184TTG14GENICheterozygous46799940
186965518469655185G-14GENICpossibly homozygous46746096
186965547669655477GA17GENICpossibly homozygous46746097
186965578669655787AG10GENIChomozygous46746098
186965601169656012AG10GENIChomozygous46746099
186965608369656084TC8GENIChomozygous46746100
186965615669656157AG7GENICpossibly homozygous46746101
186965630869656309CG17GENIChomozygous46746102
186965662369656624AG14GENIChomozygous46746103
186965685369656854AG10GENIChomozygous46746104
186965694469656945GA21GENICpossibly homozygous46746105