chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175466468175466469AG72GENIChomozygous143800097
1175466605175466606AT73GENIChomozygous143800098
1175466622175466623TC79GENIChomozygous143800099
1175466672175466687TAACTCAGCCCTAGC70GENIChomozygous143743429
1175466767175466768GT65GENIChomozygous143800100
1175467044175467045AG70GENICpossibly homozygous135753531
1175467109175467110TC70GENIChomozygous135753532
1175470200175470201GC69GENIChomozygous135753536
1175471446175471447GT57GENICpossibly homozygous143800101
1175474726175474727GA75GENIChomozygous135753540
1175474899175474900CT76GENIChomozygous143800102
1175476296175476297CT68GENIChomozygous143800103
1175476780175476781TC61GENIChomozygous135753541
1175479101175479102TC58GENIChomozygous135753544
1175480848175480848TA55GENIChomozygous143743430
1175482638175482639AG49GENIChomozygous143800104
1175484112175484113TA57GENIChomozygous135753550
1175484245175484246GT65GENIChomozygous143800105
1175484721175484722GA84GENIChomozygous143800106
1175484781175484782CT79GENIChomozygous135753552
1175487333175487334AG72GENIChomozygous135753555
1175487412175487413CT61GENIChomozygous135753556
1175487729175487730CA55GENICpossibly homozygous135753557
1175487730175487731AG55GENICpossibly homozygous135753558
1175488959175488960CT65GENIChomozygous135753561
1175489724175489725TG77GENIChomozygous135753563
1175490874175490875TC58GENIChomozygous135753566
1175492075175492075T70GENIChomozygous143743431
1175492877175492878GA39GENIChomozygous143800107
1175492997175492998AG53GENIChomozygous135753576