chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1199019349199019350CT27GENIChomozygous109532754
1199020357199020358AG25GENIChomozygous108499324
1199021116199021117CG27GENIChomozygous108499326
1199023810199023811CT21GENIChomozygous108499328
1199023914199023915AC19GENIChomozygous108499331
1199024133199024134CA17GENIChomozygous108499333
1199025358199025359GC22GENIChomozygous109532755
1199026031199026032CG24GENIChomozygous109532756
1199026133199026134AG12GENIChomozygous109532757
1199028612199028613AC31GENIChomozygous108499337
1199029028199029029TC22GENIChomozygous108499339
1199029324199029325CT21GENIChomozygous109532758
1199029404199029405TC24GENICpossibly homozygous109532759
1199029433199029434TC21GENICheterozygous109532760
1199029434199029435GA21GENICpossibly homozygous109532761
1199030002199030003AG9GENIChomozygous109532762
1199030565199030566TC12GENIChomozygous109532763
1199030597199030598AG10GENIChomozygous108499345
1199030795199030796AG21GENIChomozygous108499347
1199031955199031956AG19GENIChomozygous108499349
1199029941199029942CG16GENIChomozygous109055895