chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173296161932961620TC60GENICpossibly homozygous111031270
173296281732962818CT53GENICpossibly homozygous111031272
173296362032963621TA77GENIChomozygous111031274
173296399332963994AG54GENIChomozygous111031276
173296404932964050AG47GENIChomozygous111031278
173296560232965603GA68GENICheterozygous119337183
173296561032965611TA70GENICheterozygous119337185