chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5138921436138921437CA29GENIChomozygous71081481
5138921465138921466CG27GENIChomozygous71081485
5138922850138922851GA39GENICpossibly homozygous71960132
5138923118138923119CA20GENIChomozygous71081489
5138924303138924304GA16GENIChomozygous71960135
5138927754138927755CT30GENIChomozygous71960138
5138928626138928627GT28GENIChomozygous71960141
5138923102138923103GC4GENIChomozygous71616019
5138924804138924805CT26GENIChomozygous71804465