chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46908890869088909TC11GENIChomozygous72764067
46908902669089027TG27GENICpossibly homozygous72764069
46908913269089133CT28GENICpossibly homozygous71990772
46908900269089003GC20GENICheterozygous73895583
46908988869089889CA15GENICpossibly homozygous70798659
46908988969089890CG14GENICpossibly homozygous70798662
46909011269090113AG32GENIChomozygous70798665
46909025269090253CA19GENIChomozygous70798668
46909104369091044GT27GENIChomozygous70798674