chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
45781155157811552AG9GENIChomozygous57322240
45781202057812021AAT13GENIChomozygous57322242
45781274557812746CT7GENIChomozygous57930854
45781318357813184CA10GENICpossibly homozygous56909132
45781795257817953CCAAAA7GENICheterozygous58443656
45781799357817994A-8GENICpossibly homozygous58464696
45781818657818187GA22GENIChomozygous56909138
45781827257818273CCT11GENICpossibly homozygous57322246
45781827457818275T-11GENICheterozygous58464700
45781837457818375CCT13GENIChomozygous56909141
45781842657818427AG22GENIChomozygous57930856
45781858857818589GT21GENIChomozygous56909142
45781859457818595CT21GENIChomozygous56909143
45781866157818662GA25GENIChomozygous57930858
45781913757819138A-35GENIChomozygous56909145
45781915057819151AG32GENIChomozygous56909146
45781930557819306CA24GENIChomozygous56909147
45781978057819781GA24GENIChomozygous56909148
45781981657819817T-30GENIChomozygous56909149
45782029657820297GT17GENIChomozygous57930860
45782038757820388TC31GENIChomozygous56909150
45782148057821481GT35GENIChomozygous57930862