chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157376764157376765CT60GENICpossibly homozygous112906045
4157376776157376777TC58GENICheterozygous112906047
4157376780157376781TC59GENICheterozygous112906049
4157378488157378489GA59GENIChomozygous112906051
4157380741157380742GA28GENIChomozygous112906053