chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46908913269089133CT31GENIChomozygous71990772
46908988869089889CA29GENIChomozygous70798659
46908988969089890CG29GENIChomozygous70798662
46909011269090113AG22GENIChomozygous70798665
46909025269090253CA37GENIChomozygous70798668
46909104369091044GT32GENIChomozygous70798674
46909215069092151TC22GENICpossibly homozygous71990774
46909216369092164AG21GENICpossibly homozygous71990776