chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145377793145377794CG14GENIChomozygous112870837
4145377958145377959CT8GENIChomozygous112870838
4145378139145378140GC15GENIChomozygous112870839
4145380064145380065AG15GENIChomozygous119281650
4145380893145380894GA27GENIChomozygous112870842
4145381300145381301AG31GENIChomozygous112870843
4145381344145381345GA24GENICpossibly homozygous112870844
4145382075145382076TC20GENIChomozygous112870845
4145385904145385905CT15GENIChomozygous112870848
4145386110145386111GA21GENIChomozygous112870849
4145386860145386861AC22GENIChomozygous112870851
4145387719145387720AG21GENIChomozygous112870852
4145388150145388151CT26GENIChomozygous112870855