chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46901273369012736CAT12GENICheterozygous73086288
46901298869012989TA20GENIChomozygous71537746
46901319669013197CT15GENIChomozygous70798263
46901325669013257CG7GENIChomozygous71537748
46901341569013416CA13GENIChomozygous71537750
46901341669013417CT12GENIChomozygous71537752
46901352169013522AG7GENIChomozygous71537754
46901362869013629AG15GENIChomozygous71537755
46901375069013751CT14GENIChomozygous71537757
46901379169013793AG5GENIChomozygous73086291
46901399069013991CA17GENIChomozygous71537759
46901408969014090AC10GENIChomozygous71537763
46901447769014478CA24GENIChomozygous71537767
46901450869014509GA10GENIChomozygous70798266
46901504169015042AG9GENIChomozygous71537775
46901514469015145GA29GENIChomozygous71537777
46901384969013850CA11GENIChomozygous71990646