chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46901298869012989TA18GENIChomozygous71537746
46901319669013197CT25GENIChomozygous70798263
46901325669013257CG33GENIChomozygous71537748
46901341569013416CA25GENIChomozygous71537750
46901341669013417CT25GENIChomozygous71537752
46901352169013522AG18GENIChomozygous71537754
46901362869013629AG37GENIChomozygous71537755
46901375069013751CT21GENIChomozygous71537757
46901384969013850CA25GENIChomozygous71990646
46901399069013991CA17GENIChomozygous71537759
46901408969014090AC25GENIChomozygous71537763
46901418969014190CA8GENIChomozygous71990648
46901421369014214CG10GENIChomozygous71537765
46901447769014478CA25GENIChomozygous71537767
46901475469014755AG3GENIChomozygous72584599
46901488269014883CT22GENIChomozygous71537771
46901504169015042AG32GENIChomozygous71537775
46901514469015145GA54GENIChomozygous71537777