chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1102103140102103141CT13GENIChomozygous108901595
1102103368102103369TC38GENIChomozygous108901596
1102103996102103997CT26GENIChomozygous108901599
1102104070102104071GA21GENIChomozygous108901600
1102104254102104255CT30GENIChomozygous108901601
1102104449102104450GC27GENIChomozygous108901602
1102105142102105143AG43GENIChomozygous108901603
1102105163102105164AG38GENIChomozygous108901604
1102105319102105320CT35GENIChomozygous108901605
1102106176102106177CT28GENIChomozygous108901606