chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1170474506170474507CA44GENIChomozygous974627246
1170476124170476125AC19GENIChomozygous974627247
1170481166170481167TG13GENIChomozygous974627248
1170483030170483031TC21GENIChomozygous974627249
1170484498170484499CA23GENIChomozygous974627250
1170496625170496626AT41GENIChomozygous974627251
1170497569170497570GA18GENIChomozygous974627252
1170505859170505860AG30GENIChomozygous974627253
1170506843170506844GT28GENIChomozygous974627254
1170518919170518920GC15GENIChomozygous974627255
1170527080170527081TC42GENIChomozygous974627256
1170543323170543324TC27GENIChomozygous974627257
1170543893170543894AG21GENIChomozygous974627258
1170544857170544858GT40GENIChomozygous974627259
1170545941170545942GA14GENIChomozygous974627260
1170553088170553089TC27GENIChomozygous974627261
1170555934170555935AG15GENIChomozygous974627262
1170558673170558674TA29GENICheterozygous974627263
1170567686170567687TC41GENIChomozygous974627264