chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117457980117457981AG30GENIChomozygous889863433
8117459094117459095TC15GENICheterozygous889863434
8117460884117460885CT25GENIChomozygous889863435
8117461269117461270AT6GENIChomozygous889863436
8117462087117462088AG20GENIChomozygous889863437
8117462354117462355CT16GENIChomozygous889863438
8117462477117462478AG15GENIChomozygous889863439
8117462488117462489AG13GENIChomozygous889863440
8117462614117462615CT13GENIChomozygous889863441
8117462629117462630AG13GENIChomozygous889863442
8117462692117462693CT17GENIChomozygous889863443
8117463605117463606CT14GENIChomozygous889863444
8117463853117463854CT20GENIChomozygous889863445
8117464433117464434GA8GENIChomozygous889863446
8117464601117464602TC16GENIChomozygous889863447
8117465468117465469GT14GENIChomozygous889863448
8117466249117466250AC29GENIChomozygous889863449
8117466294117466295TC24GENIChomozygous889863450
8117466327117466328CA29GENIChomozygous889863451
8117466724117466725AG36GENIChomozygous889863452
8117466759117466760CT31GENIChomozygous889863453
8117466987117466988CT17GENIChomozygous889863454
8117467675117467676TC15GENIChomozygous889863455
8117469362117469363TC17GENIChomozygous889863456
8117470014117470015TC7GENIChomozygous889863457
8117470442117470443GC4GENIChomozygous889863458
8117470941117470942CG5GENICheterozygous889863459
8117471283117471284TC20GENIChomozygous889863460
8117471357117471358AT26GENIChomozygous889863461
8117472454117472455GA15GENIChomozygous889863462
8117475110117475111CA10GENIChomozygous889863463