chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46908913269089133CT16GENICpossibly homozygous71990772
46908988869089889CA12GENIChomozygous70798659
46908988969089890CG12GENIChomozygous70798662
46909011269090113AG14GENIChomozygous70798665
46909025269090253CA17GENICpossibly homozygous70798668
46909104369091044GT15GENICpossibly homozygous70798674
46909215069092151TC11GENICpossibly homozygous71990774
46909216369092164AG9GENICheterozygous71990776