chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136696987136696988CA8GENICpossibly homozygous56682784
5136697096136697097CCA14GENIChomozygous56456411
5136697354136697355GA8GENIChomozygous56682785
5136698195136698200TCCTA-----5GENICheterozygous56682786
5136698752136698753CT8GENIChomozygous56682787
5136700834136700836AA--2GENIChomozygous56682788
5136701671136701672GT5GENIChomozygous56456418
5136701979136701980A-16GENICheterozygous56354820
5136703257136703258A-13GENIChomozygous56682789