chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170474506170474507CA32GENIChomozygous992676191
1170476124170476125AC21GENIChomozygous992676192
1170477009170477010AT23GENICheterozygous992676193
1170481166170481167TG10GENIChomozygous992676194
1170483030170483031TC28GENIChomozygous992676195
1170484498170484499CA25GENIChomozygous992676196
1170496625170496626AT23GENIChomozygous992676197
1170505859170505860AG22GENIChomozygous992676198
1170506843170506844GT31GENIChomozygous992676199
1170518919170518920GC15GENIChomozygous992676200
1170520957170520958GA22GENIChomozygous992676201
1170527080170527081TC32GENIChomozygous992676202
1170543323170543324TC32GENIChomozygous992676203
1170544857170544858GT26GENIChomozygous992676204
1170553088170553089TC28GENIChomozygous992676205
1170555934170555935AG30GENIChomozygous992676206
1170558673170558674TA17GENICpossibly homozygous992676207
1170567686170567687TC27GENIChomozygous992676208
1170570113170570114AG29GENIChomozygous992676209