chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4124012739124012740CT19GENIChomozygous126022892
4124012852124012853GT15GENIChomozygous126022893
4124012902124012903AT19GENIChomozygous126022894
4124012932124012933AT8GENIChomozygous126022895
4124012941124012942GT5GENIChomozygous126022896
4124012947124012948GT9GENIChomozygous126022897
4124021726124021727AC14GENIChomozygous126022898
4124023484124023485AG17GENICpossibly homozygous126022899
4124023609124023610GT22GENIChomozygous126022900
4124023711124023712AG9GENIChomozygous126022901