chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141173097141173098T19GENIChomozygous127438827
1141174076141174077A18GENICheterozygous127438828
1141175989141175990TG25GENIChomozygous108260251
1141178277141178278CT26GENIChomozygous108260253
1141180488141180489TC16GENIChomozygous108260255
1141180561141180562AG10GENIChomozygous108260257
1141181799141181801TA18GENIChomozygous127438829
1141182185141182186CT15GENIChomozygous108260259
1141182361141182362CT21GENIChomozygous108260261
1141182389141182390TG20GENIChomozygous108260263
1141182724141182725TC20GENIChomozygous108260265
1141183357141183357AGCTTGGTCTCGAGCCTGGCA22GENIChomozygous127438830
1141184886141184887TA20GENIChomozygous108260267
1141185562141185563AG18GENIChomozygous108260269
1141185906141185907CT20GENIChomozygous108260271
1141186546141186547TG9GENIChomozygous108743821
1141186604141186605TA14GENIChomozygous108260273
1141186614141186615AG16GENIChomozygous108260275
1141187219141187220CA30GENIChomozygous108260277
1141187564141187565CT27GENIChomozygous108260279
1141188724141188725TC29GENIChomozygous108260281