chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1175466468175466469AG14GENIChomozygous143800097
1175466605175466606AT17GENIChomozygous143800098
1175466622175466623TC13GENIChomozygous143800099
1175466672175466687TAACTCAGCCCTAGC13GENIChomozygous143743429
1175466767175466768GT27GENIChomozygous143800100
1175467044175467045AG17GENIChomozygous135753531
1175467109175467110TC11GENIChomozygous135753532
1175470200175470201GC18GENIChomozygous135753536
1175471446175471447GT30GENIChomozygous143800101
1175474726175474727GA34GENIChomozygous135753540
1175474899175474900CT27GENIChomozygous143800102
1175476296175476297CT17GENIChomozygous143800103
1175476780175476781TC21GENIChomozygous135753541
1175479101175479102TC13GENIChomozygous135753544
1175480848175480848TA26GENIChomozygous143743430
1175482638175482639AG15GENIChomozygous143800104
1175484112175484113TA23GENIChomozygous135753550
1175484245175484246GT22GENIChomozygous143800105
1175484721175484722GA22GENIChomozygous143800106
1175484781175484782CT21GENIChomozygous135753552
1175487333175487334AG21GENIChomozygous135753555
1175487412175487413CT22GENIChomozygous135753556
1175487729175487730CA21GENIChomozygous135753557
1175487730175487731AG21GENIChomozygous135753558
1175488959175488960CT22GENIChomozygous135753561
1175489724175489725TG27GENIChomozygous135753563
1175490874175490875TC21GENIChomozygous135753566
1175492075175492075T19GENIChomozygous143743431
1175492877175492878GA16GENIChomozygous143800107
1175492997175492998AG22GENIChomozygous135753576