chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46901298869012989TA21GENIChomozygous71537746
46901319669013197CT6GENIChomozygous70798263
46901325669013257CG9GENIChomozygous71537748
46901341569013416CA11GENIChomozygous71537750
46901341669013417CT11GENIChomozygous71537752
46901352169013522AG4GENIChomozygous71537754
46901362869013629AG10GENIChomozygous71537755
46901375069013751CT12GENIChomozygous71537757
46901384969013850CA6GENIChomozygous71990646
46901399069013991CA9GENIChomozygous71537759
46901408969014090AC9GENIChomozygous71537763
46901418969014190CA5GENIChomozygous71990648
46901421369014214CG5GENIChomozygous71537765
46901488269014883CT10GENICpossibly homozygous71537771
46901514469015145GA24GENIChomozygous71537777