chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171905856419058565GT28GENIChomozygous111176121
171905976219059763CT32GENIChomozygous111296823
171906017319060174TA27GENIChomozygous111176125
171906050619060507TC34GENIChomozygous111296824
171906054119060542CT37GENIChomozygous111296825
171906124919061250AG36GENIChomozygous111176129
171906157019061571CT28GENIChomozygous111296826
171906196819061969TC37GENIChomozygous111176139
171906232219062323AG38GENIChomozygous111176141
171906249919062500GA32GENIChomozygous111176143
171906289819062899AG37GENIChomozygous111176147