chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175134918175134919GA12GENICpossibly homozygous60956077
1175135048175135049AATTC17GENIChomozygous60956079
1175135180175135181CA15GENIChomozygous60956081
1175135222175135223AG18GENIChomozygous60956083
1175135301175135302AG10GENIChomozygous60956085
1175135374175135375TA13GENIChomozygous60956087
1175135592175135593TC38GENICpossibly homozygous60956089
1175135876175135877AG27GENIChomozygous60956091