chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136125800136125801GA74GENIChomozygous112839386
4136126019136126020TA60GENICpossibly homozygous112839388
4136126158136126159GA89GENIChomozygous112839390
4136126170136126171GA83GENIChomozygous112839392
4136126205136126206AT79GENIChomozygous112839394
4136126231136126232AG77GENIChomozygous112839396
4136126253136126254TC69GENIChomozygous112839398
4136126364136126365AC65GENIChomozygous112839400
4136126760136126761AG50GENICpossibly homozygous112839402
4136126840136126841TC29GENIChomozygous112839404
4136126895136126896AG40GENIChomozygous112839405
4136127028136127029AG68GENIChomozygous112839407