chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3159996063159996064TC22GENIChomozygous111791119
3159996198159996199AG33GENIChomozygous111791121
3159996625159996626AG19GENIChomozygous111791123
3159996640159996641CT16GENIChomozygous111791125
3159996681159996682GA27GENIChomozygous111791127
3159998011159998012AG13GENIChomozygous111791129
3159998102159998103AG15GENIChomozygous111791131
3160000272160000273GA19GENIChomozygous111791133
3160005018160005019CT22GENIChomozygous111791135
3160008150160008151CG39GENIChomozygous111791137
3160009225160009226CT18GENIChomozygous111791138
3160010164160010165AG36GENIChomozygous111791140
3160010762160010763GC27GENIChomozygous111791142
3160011322160011323CA19GENIChomozygous111791144
3160011765160011766AG21GENIChomozygous111791146
3160013805160013806AG30GENIChomozygous111791148
3160014125160014126AT18GENIChomozygous111791150
3160014630160014631GA23GENIChomozygous111791152