chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79791739697917397TA17GENIChomozygous116215490
79791815897918159AC8GENIChomozygous116215491
79791861597918616CT12GENIChomozygous116215492
79791880197918802AC20GENIChomozygous116215493
79791884097918841TC31GENIChomozygous116215494
79791924997919250AG13GENIChomozygous116215495
79791965397919654GT6GENIChomozygous126536044
79791965597919656GA5GENIChomozygous126546380
79791967597919676TG8GENIChomozygous126536045
79791969897919699TG10GENIChomozygous126536046
79791981497919815GC24GENIChomozygous126536047
79791986597919866CT8GENIChomozygous126536048
79791991697919917CG9GENIChomozygous126536049
79791992897919929CG11GENIChomozygous126536050
79791996697919967AT13GENIChomozygous126546381
79792245797922458CT17GENIChomozygous116215496
79792590997925910AG17GENIChomozygous116215497
79793671897936719CT21GENIChomozygous126585259
79794091797940918CT4GENIChomozygous126585260