chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141172521141172522GA34GENIChomozygous108936509
1141174997141174998CT23GENIChomozygous109327497
1141176570141176571TC27GENIChomozygous108936512
1141177656141177657TC21GENIChomozygous108936513
1141177807141177808TA35GENIChomozygous108936514
1141180561141180562AG5GENIChomozygous108260257
1141175989141175990TG26GENIChomozygous108260251
1141182361141182362CT21GENIChomozygous108260261
1141182389141182390TG27GENIChomozygous108260263
1141182724141182725TC30GENIChomozygous108260265
1141184886141184887TA16GENIChomozygous108260267
1141185819141185820GA34GENIChomozygous109327498
1141185906141185907CT25GENIChomozygous108260271
1141186604141186605TA15GENIChomozygous108260273
1141186614141186615AG14GENIChomozygous108260275
1141187219141187220CA14GENIChomozygous108260277
1141187564141187565CT7GENIChomozygous108260279
1141188611141188612CT9GENICpossibly homozygous109327499