chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
164946345049463451GC39GENIChomozygous111811107
164946367849463679CT36GENICheterozygous119117640
164946399449463995TG20GENIChomozygous111811109
164946417349464174GT17GENIChomozygous111980849
164946454449464545TC21GENIChomozygous111811111
164946476449464765CT39GENIChomozygous111811113
164946476849464769AG38GENIChomozygous111811115
164946480349464804TC40GENIChomozygous111811117
164946483249464833AG51GENIChomozygous111811119
164946513049465131CT56GENIChomozygous111811121
164946532849465329AT19GENIChomozygous111811123
164946539549465396AG29GENIChomozygous111811125
164946542249465423AG34GENIChomozygous111811127
164946544349465444GT38GENIChomozygous111811129
164946552749465528GA47GENIChomozygous111811131