chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1256102280256102281TC69GENIChomozygous108620034
1256102527256102528GT68GENIChomozygous120693634
1256104172256104173CT70GENIChomozygous108620038
1256104389256104390TC53GENIChomozygous108620040
1256104523256104524TC47GENICpossibly homozygous108620042
1256104713256104714AC54GENICpossibly homozygous108620044
1256104958256104959AG63GENICpossibly homozygous108620046
1256105539256105540AG40GENIChomozygous108620052
1256105554256105555CT44GENIChomozygous108620054
1256106108256106109CT52GENICpossibly homozygous108620055
1256107227256107228CT44GENIChomozygous108620059
1256105621256105631TAGCTTCCTG43GENIChomozygous127505335
1256107548256107549T42GENIChomozygous127505336
1256105576256105578AA35GENIChomozygous127505334