chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141172521141172522GA25GENIChomozygous108936509
1141174997141174998CT24GENIChomozygous109327497
1141175989141175990TG23GENICpossibly homozygous108260251
1141176570141176571TC15GENIChomozygous108936512
1141177656141177657TC14GENIChomozygous108936513
1141177807141177808TA18GENIChomozygous108936514
1141180561141180562AG18GENIChomozygous108260257
1141182361141182362CT18GENIChomozygous108260261
1141182389141182390TG17GENIChomozygous108260263
1141182724141182725TC22GENIChomozygous108260265
1141184886141184887TA20GENIChomozygous108260267
1141185562141185563AG32GENIChomozygous108260269
1141185819141185820GA30GENIChomozygous109327498
1141187564141187565CT15GENIChomozygous108260279
1141176022141176023GC17GENIChomozygous120906468
1141176030141176031CT18GENIChomozygous120906469
1141180844141180845AT15GENIChomozygous120505687
1141185906141185907CT18GENIChomozygous108260271
1141186604141186605TA14GENIChomozygous108260273
1141186614141186615AG17GENIChomozygous108260275
1141187219141187220CA15GENIChomozygous108260277
1141188724141188725TC4GENIChomozygous108260281