chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1134882661134882662A42GENIChomozygous141169743
1134883941134883942TC63GENIChomozygous135673098
1134885446134885447T30GENIChomozygous135430256
1134886149134886150CG28GENIChomozygous144556258
1134886556134886557TA51GENIChomozygous135673105
1134888565134888566CT52GENIChomozygous135673108
1134889578134889579GC57GENIChomozygous135673109
1134891165134891166AT52GENIChomozygous135673112
1134894063134894064GA43GENIChomozygous141252214
1134886677134886678GA42GENIChomozygous141252211
1134887250134887251GT52GENIChomozygous141252212
1134891044134891045GA49GENIChomozygous141252213
1134894148134894149GC46GENIChomozygous135673115
1134894438134894439AG46GENIChomozygous135673116
1134896147134896148GA33GENIChomozygous141252215
1134896268134896269AG32GENIChomozygous141252216
1134896559134896560GA43GENIChomozygous141252217
1134896842134896843TC45GENIChomozygous135673117
1134897163134897164GA48GENIChomozygous141252218
1134897235134897236GA55GENIChomozygous135673119
1134897343134897344AG49GENIChomozygous135673120
1134897409134897409TT46GENIChomozygous135430258
1134899002134899003GC32GENIChomozygous135673122
1134899221134899222TC48GENIChomozygous135673123
1134899627134899631TTTA16GENIChomozygous135430260
1134900623134900623CT20GENICheterozygous135430262
1134901138134901139TG50GENICpossibly homozygous141252219
1134901145134901148GCT48GENICpossibly homozygous141169744
1134902135134902137CT26GENIChomozygous135430264
1134902137134902138GA26GENIChomozygous135673126
1134902420134902421TC59GENIChomozygous135673127
1134902453134902466GCTCGGGAAGTTT54GENIChomozygous141169745
1134903126134903127TC78GENIChomozygous135673130
1134905194134905195AG47GENIChomozygous135673133
1134906079134906080TC42GENIChomozygous141252220
1134906107134906108GA39GENIChomozygous141252221
1134906372134906373TC57GENIChomozygous135673136
1134906387134906388TG54GENIChomozygous135673137
1134906408134906409AC53GENIChomozygous135673138
1134908885134908886CT44GENIChomozygous141252222