chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3164274901164274902TC20GENIChomozygous111807032
3164276487164276488GA55GENICpossibly homozygous111807034
3164276573164276574GT43GENIChomozygous111807036
3164277032164277033AG40GENIChomozygous111807038
3164277133164277134CA43GENICpossibly homozygous111807040
3164277471164277472AG53GENIChomozygous111807042
3164277621164277622TC39GENIChomozygous111807044
3164278026164278027AG51GENIChomozygous111807046
3164278135164278136GA49GENICpossibly homozygous111807048