chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172111420921114210GA17GENIChomozygous125543967
172111428421114285CT20GENIChomozygous125500719
172111433921114340TG10GENIChomozygous125500720
172111440721114408TC14GENIChomozygous125500721
172111449821114499CT11GENIChomozygous125500722
172111519121115192CT17GENIChomozygous125543968
172111620321116204GC21GENIChomozygous125500723
172111622721116228AG15GENIChomozygous125500724
172111639821116399TC21GENIChomozygous125500725
172111680021116801TC17GENIChomozygous125500726
172111687321116874CT4GENIChomozygous125500727
172111703521117036AT16GENIChomozygous125500728
172111705421117055TC12GENIChomozygous125500729
172111712321117124TC21GENIChomozygous125500730
172111752721117528GC19GENIChomozygous125543969
172111770121117702TC15GENIChomozygous125500733
172111780921117810AG16GENIChomozygous125500734
172111798421117985TC13GENIChomozygous125500735
172111811121118112AG6GENIChomozygous125500736
172111890221118903TC22GENIChomozygous125500737
172111897321118974AG16GENIChomozygous125500738
172111902421119025CA17GENIChomozygous125500739
172111927721119278TA16GENIChomozygous125500740
172111952821119529GA18GENIChomozygous125543970
172111963021119631TC11GENIChomozygous125543971