chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172690017826900179T7GENICpossibly homozygous403411171
172690017826900179TG7GENICheterozygous403411172
172691460526914606A8GENICheterozygous403411174
172691460526914606AT8GENICheterozygous403411175
172692196026921960AC17GENIChomozygous140017262
172698770726987708GC15GENICheterozygous146569776