chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107999234979992350G69GENIChomozygous144857141
107999626979996270TG47GENICpossibly homozygous144872034
107999757379997573T52GENIChomozygous138693292
107999896479998965CT45GENIChomozygous144872035
107999924179999242TC47GENIChomozygous138831090
108000690980006909CT49GENIChomozygous143433788