chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89707631397076314GA67GENIChomozygous116854974
89707651897076519TC84GENICpossibly homozygous116854975
89707657397076574CT63GENICpossibly homozygous116854976
89707689097076891CT51GENIChomozygous116854977
89707701397077014TC48GENIChomozygous116854978
89707719797077198TA33GENIChomozygous116591236
89707831297078313AT43GENIChomozygous116854979
89707904897079049CT75GENIChomozygous116854980
89707919797079198CT72GENICpossibly homozygous116854981
89707950697079507CT40GENIChomozygous116591242
89707961297079613GA55GENIChomozygous116591244
89707987397079874GA66GENIChomozygous116591246
89707989397079894GT67GENIChomozygous116591248
89707993397079934TC65GENIChomozygous116591250
89708008897080089AG67GENIChomozygous116591254
89708014197080142AG57GENICpossibly homozygous116591256
89708018297080183GA52GENIChomozygous116591258
89708053097080531GA68GENIChomozygous116854982
89708059197080592CA61GENICpossibly homozygous116854983
89708182397081824TG49GENIChomozygous116854984
89708279997082800GC49GENIChomozygous116591262
89708280597082806AG50GENICpossibly homozygous116591264