chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159996063159996064TC28GENIChomozygous111791119
3159996198159996199AG38GENIChomozygous111791121
3159996625159996626AG26GENIChomozygous111791123
3159996640159996641CT27GENIChomozygous111791125
3159996681159996682GA27GENIChomozygous111791127
3159998011159998012AG25GENIChomozygous111791129
3159998102159998103AG30GENIChomozygous111791131
3160000272160000273GA24GENIChomozygous111791133
3160005018160005019CT19GENIChomozygous111791135
3160008150160008151CG30GENICpossibly homozygous111791137
3160009225160009226CT29GENICpossibly homozygous111791138
3160010164160010165AG34GENIChomozygous111791140
3160010762160010763GC22GENIChomozygous111791142
3160011322160011323CA20GENIChomozygous111791144
3160011765160011766AG27GENIChomozygous111791146
3160013805160013806AG27GENIChomozygous111791148
3160014125160014126AT32GENICpossibly homozygous111791150
3160014630160014631GA29GENIChomozygous111791152