chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46901273369012736CAT9GENIChomozygous73086288
46901286869012869TG4GENIChomozygous73784109
46901298869012989TA14GENIChomozygous71537746
46901319669013197CT12GENIChomozygous70798263
46901325669013257CG4GENIChomozygous71537748
46901341569013416CA11GENIChomozygous71537750
46901341669013417CT11GENIChomozygous71537752
46901352169013522AG11GENIChomozygous71537754
46901362869013629AG18GENIChomozygous71537755
46901375069013751CT25GENIChomozygous71537757
46901399069013991CA21GENIChomozygous71537759
46901408969014090AC18GENIChomozygous71537763
46901447769014478CA31GENIChomozygous71537767
46901450869014509GA10GENIChomozygous70798266
46901504169015042AG11GENIChomozygous71537775
46901514469015145GA27GENIChomozygous71537777
46901384969013850CA6GENIChomozygous71990646