chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170474506170474507CA25GENIChomozygous108376096
1170476124170476125AC19GENIChomozygous108376098
1170481166170481167TG12GENIChomozygous108376102
1170483030170483031TC14GENIChomozygous108376104
1170484498170484499CA18GENIChomozygous108376106
1170496625170496626AT25GENIChomozygous108376149
1170497569170497570GA16GENIChomozygous108376151
1170505859170505860AG16GENIChomozygous108376153
1170506843170506844GT29GENIChomozygous108376155
1170518919170518920GC15GENIChomozygous108376159
1170520957170520958GA22GENIChomozygous108376161
1170527080170527081TC25GENIChomozygous108376165
1170543323170543324TC27GENIChomozygous108376173
1170543893170543894AG24GENIChomozygous108958863
1170544857170544858GT25GENIChomozygous108376175
1170545941170545942GA16GENIChomozygous108958864
1170553088170553089TC17GENIChomozygous108376177
1170555934170555935AG20GENIChomozygous108376179
1170566344170566345GT8GENICheterozygous120730110
1170567686170567687TC26GENIChomozygous108376183