chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184461220744612208AT20GENICpossibly homozygous46430157
184462082444620825CT5GENIChomozygous46430159
184462310444623105CCA17GENIChomozygous46430161
184462604544626049TGTG----7GENICheterozygous46430163
184462604744626049TG--7GENICheterozygous46430165
184462949144629492AG28GENIChomozygous46430166