chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101371171613711717AG53GENIChomozygous51621962
101371172613711727CT52GENIChomozygous51621963
101371223613712237TA28GENIChomozygous51621964
101371288213712883TC36GENIChomozygous51621965
101371371413713715GA31GENIChomozygous51621966
101371492113714922GC22GENIChomozygous51621967
101371497413714975GA26GENIChomozygous51621968
101371533613715337CCTG8GENICpossibly homozygous51621969