chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76123304861233049GC22GENICpossibly homozygous625321267
76123319561233196GT7GENIChomozygous625321268
76123354361233544TC4GENIChomozygous625321269
76123388861233889AT12GENICpossibly homozygous625321270
76123398661233987TC15GENIChomozygous625321271
76123408161234082CG9GENIChomozygous625321272
76123440061234401AT19GENICpossibly homozygous625321273
76123443761234438CT13GENICpossibly homozygous625321274
76123478061234781CT22GENIChomozygous625321275
76123517761235178AG21GENICpossibly homozygous625321276
76123543161235432TG15GENIChomozygous625321277
76123601861236019CT21GENICpossibly homozygous625321278
76123608261236083AC12GENIChomozygous625321279
76123618961236190TC19GENICheterozygous625321280
76123636861236369CT24GENICpossibly homozygous625321281
76123646961236470AG28GENIChomozygous625321282
76123656761236568GA7GENIChomozygous625321283