chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101112112711121128CT26GENIChomozygous116494256
101112127111121272CA28GENIChomozygous116494258
101112223911122240CT43GENIChomozygous116494260
101112306411123065AG42GENIChomozygous116494262
101112426911124270GA37GENIChomozygous116494264
101112436311124364GA25GENIChomozygous116494266
101112535811125359TC31GENIChomozygous116494268
101112551811125519GA31GENIChomozygous116494270
101112926111129262GT21GENICpossibly homozygous117981298
101113008511130086TC34GENIChomozygous116494272
101113148011131481CA31GENIChomozygous116494274
101112981311129814GA13GENICheterozygous118073747