chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
172111428421114285CT22GENIChomozygous125500719
172111433921114340TG17GENIChomozygous125500720
172111440721114408TC23GENIChomozygous125500721
172111449821114499CT24GENIChomozygous125500722
172111620321116204GC27GENIChomozygous125500723
172111622721116228AG32GENIChomozygous125500724
172111639821116399TC27GENIChomozygous125500725
172111680021116801TC16GENIChomozygous125500726
172111687321116874CT4GENIChomozygous125500727
172111703521117036AT21GENIChomozygous125500728
172111705421117055TC17GENIChomozygous125500729
172111712321117124TC20GENIChomozygous125500730
172111745321117454GA15GENIChomozygous125500731
172111760321117604GA27GENIChomozygous125500732
172111770121117702TC21GENIChomozygous125500733
172111780921117810AG34GENIChomozygous125500734
172111798421117985TC24GENIChomozygous125500735
172111811121118112AG14GENIChomozygous125500736
172111890221118903TC12GENIChomozygous125500737
172111897321118974AG10GENIChomozygous125500738
172111902421119025CA14GENIChomozygous125500739
172111927721119278TA29GENIChomozygous125500740
172112054321120544TC4GENIChomozygous125500741
172112062221120623TC17GENIChomozygous125500742