chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18224903182249032AG15GENIChomozygous108877644
18224928382249284TG21GENIChomozygous108877645
18224959582249596CT35GENIChomozygous108877646
18225199482251995AG18GENIChomozygous108877647
18225200182252002CG21GENIChomozygous108877648
18225202082252021TC21GENIChomozygous108877649
18225270882252709CT26GENIChomozygous108877650
18225330882253309AG26GENIChomozygous108877651
18225340882253409AG12GENIChomozygous108877652
18225568782255688GT27GENIChomozygous108877653
18225572382255724TC28GENIChomozygous108877654
18225601882256019TC28GENIChomozygous108877655
18225770682257707AG14GENIChomozygous108877656
18225782582257826CT8GENIChomozygous108877657
18225834282258343GA24GENIChomozygous108877658
18225933582259336TC25GENIChomozygous108877659
18225936882259369CT29GENIChomozygous108877660
18225965782259658TC28GENIChomozygous108877661
18225989682259897GA17GENIChomozygous108877662
18226240082262401AG24GENIChomozygous108877663
18226360282263603AT34GENIChomozygous108877664
18226375882263759TC28GENIChomozygous108877665
18226443182264432GA11GENIChomozygous108877666
18226447782264478TC12GENIChomozygous108877667
18226462882264629CT11GENIChomozygous108877668
18226595382265954TC19GENIChomozygous108877669