chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171058612610586127CA4GENIChomozygous110954433
171058651010586511AG19GENIChomozygous110954435
171058741010587411TG32GENIChomozygous110954437
171058779910587800GT24GENIChomozygous111231022
171058895310588954AG25GENIChomozygous110954439
171058908810589089GA38GENIChomozygous110954441
171059311210593113AG30GENIChomozygous110954443
171059332410593325CT18GENIChomozygous110954445
171059336710593368GA22GENIChomozygous110954447
171059340110593402CT21GENIChomozygous110954449
171059362610593627CT27GENIChomozygous110954451
171059377910593780CA33GENIChomozygous110954453
171059428510594286GC28GENIChomozygous110954455
171059470610594707AT16GENIChomozygous110954457
171059488410594885TA24GENIChomozygous110954459
171059493010594931CT31GENIChomozygous110954461
171059516410595165AG22GENIChomozygous110954463
171059525410595255AT22GENIChomozygous110954465
171059541210595413AG12GENIChomozygous110954467
171059546010595461CA13GENIChomozygous110954469
171059549010595491TG11GENIChomozygous110954471
171059634410596345CG29GENIChomozygous110954473
171059649610596497TC23GENIChomozygous110954475
171059690210596903CT19GENIChomozygous110954477
171059781610597817TG9GENIChomozygous110954479
171059782410597825CT8GENIChomozygous111231024
171059831610598317CA25GENIChomozygous110954483