chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117209535072095351GA5GENIChomozygous115985656
117209556572095566TC6GENIChomozygous115985658
117209567672095677GT7GENIChomozygous115985660
117209596672095967GT16GENIChomozygous115985662
117209609172096092CT2GENIChomozygous115985664
117209623372096234CT12GENIChomozygous115985666
117209680472096805GA9GENICpossibly homozygous115985668
117209718172097182AG14GENIChomozygous115985670
117209821172098212GA11GENIChomozygous115985672
117209879372098794AG5GENIChomozygous115985674
117209884472098845TC6GENIChomozygous115985676
117209885572098856GA6GENIChomozygous115985678
117209911772099118TC6GENIChomozygous115985680
117209972872099729AT9GENIChomozygous115985682
117210069872100699AT10GENIChomozygous115985684
117210132272101323AG11GENIChomozygous115985686
117210165272101653AC6GENIChomozygous115985688
117210245672102457AG9GENIChomozygous115985690