chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117457980117457981AG44GENIChomozygous964459372
8117459094117459095TC20GENIChomozygous964459373
8117460884117460885CT38GENIChomozygous964459374
8117461269117461270AT7GENICpossibly homozygous964459375
8117462087117462088AG31GENIChomozygous964459376
8117462354117462355CT25GENIChomozygous964459377
8117462477117462478AG20GENIChomozygous964459378
8117462488117462489AG19GENIChomozygous964459379
8117462614117462615CT12GENIChomozygous964459380
8117462629117462630AG9GENIChomozygous964459381
8117462692117462693CT18GENIChomozygous964459382
8117463605117463606CT25GENIChomozygous964459383
8117463853117463854CT22GENIChomozygous964459384
8117464433117464434GA13GENIChomozygous964459385
8117464601117464602TC26GENIChomozygous964459386
8117465468117465469GT31GENIChomozygous964459387
8117466249117466250AC30GENIChomozygous964459388
8117466294117466295TC34GENIChomozygous964459389
8117466327117466328CA31GENIChomozygous964459390
8117466724117466725AG39GENIChomozygous964459391
8117466759117466760CT35GENIChomozygous964459392
8117466987117466988CT27GENIChomozygous964459393
8117467476117467477TG24GENIChomozygous964459394
8117467952117467953AG18GENIChomozygous964459395
8117468864117468865CG15GENIChomozygous964459396
8117469362117469363TC29GENIChomozygous964459397
8117470014117470015TC26GENIChomozygous964459398
8117471283117471284TC37GENIChomozygous964459399
8117471357117471358AT46GENIChomozygous964459400
8117475110117475111CA18GENIChomozygous964459401