chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170474506170474507CA25GENIChomozygous108376096
1170476124170476125AC29GENIChomozygous108376098
1170481166170481167TG10GENIChomozygous108376102
1170483030170483031TC17GENIChomozygous108376104
1170484498170484499CA30GENIChomozygous108376106
1170481285170481286AG9GENICheterozygous120906611
1170496625170496626AT25GENIChomozygous108376149
1170497569170497570GA14GENIChomozygous108376151
1170518919170518920GC26GENIChomozygous108376159
1170520957170520958GA33GENIChomozygous108376161
1170527080170527081TC28GENIChomozygous108376165
1170543323170543324TC35GENIChomozygous108376173
1170543893170543894AG32GENIChomozygous108958863
1170544857170544858GT28GENIChomozygous108376175
1170545941170545942GA13GENIChomozygous108958864
1170553088170553089TC34GENIChomozygous108376177
1170555934170555935AG17GENIChomozygous108376179
1170558673170558674TA23GENICpossibly homozygous108376181
1170567686170567687TC38GENIChomozygous108376183