chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135457372054573721GA17GENIChomozygous973629105
135457374054573741AG14GENIChomozygous973629106
135457374454573745CT14GENIChomozygous973629107
135457451054574511TC8GENIChomozygous973629108
135457476154574762GC16GENIChomozygous973629109
135457536054575361GA11GENIChomozygous973629110
135457550754575508GA9GENIChomozygous973629111
135457639654576397TC21GENIChomozygous973629112
135457665554576656AG21GENIChomozygous973629113
135457669254576693CT30GENIChomozygous973629114
135457693754576938AT20GENIChomozygous973629115
135457788454577885CT6GENIChomozygous973629116
135457817754578178TC12GENIChomozygous973629117
135457910154579102AG12GENIChomozygous973629118
135457910654579107TC12GENICpossibly homozygous973629119
135457916754579168GA12GENIChomozygous973629120
135457956354579564AG9GENIChomozygous973629121
135457959354579594TC8GENIChomozygous973629122
135457975554579756AG18GENIChomozygous973629123
135457986954579870AG13GENIChomozygous973629124