chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1191678037191678038CA30GENIChomozygous109179521
1191679008191679009TC28GENIChomozygous108467518
1191680943191680944AT28GENIChomozygous109179523
1191681550191681551TG36GENIChomozygous108467522
1191682851191682852GA17GENICpossibly homozygous109179527
1191684026191684027CA25GENICpossibly homozygous109179529
1191684049191684050CA27GENICpossibly homozygous109179531
1191684409191684410CT27GENIChomozygous109179533
1191684754191684755TC29GENIChomozygous108467527
1191685419191685420TC20GENIChomozygous108467529
1191685739191685740CT18GENIChomozygous109179537