chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
996903579690358CA25GENIChomozygous117243413
996908399690840TC11GENIChomozygous117243414
996908969690896C8GENIChomozygous128678011
996909079690908C8GENIChomozygous128678012
996909329690932GC6GENIChomozygous128678013
996912549691255AG37GENIChomozygous117243415
996918299691830GA47GENIChomozygous117243416
996920299692030AC46GENICpossibly homozygous117243417
996923739692374TC46GENIChomozygous117243418
996925509692551GA45GENIChomozygous117243419
996925939692594AG42GENIChomozygous117243420
996927529692753TG41GENIChomozygous117243421
996928399692840TA32GENIChomozygous117243422
996928479692847G32GENIChomozygous128678014
996931079693108CT48GENIChomozygous117243423
996937209693721TC28GENIChomozygous117243426
996938959693896CT36GENIChomozygous117243427
996939189693919CA41GENICpossibly homozygous117243428
996943339694334GA38GENIChomozygous117455102
996943349694335AG38GENIChomozygous117455103
996944329694433TA42GENIChomozygous117243429
996946459694646AG39GENIChomozygous117243430
996952679695268CA40GENIChomozygous117243431
996953159695316TC38GENIChomozygous117243432
996954729695473TC54GENIChomozygous117243433
996972359697236CT41GENIChomozygous117243437
996975369697537CT34GENIChomozygous117243438
996982469698247AG62GENIChomozygous117243439
996983249698325AG55GENIChomozygous117243440
996984819698482TC39GENIChomozygous117243441
996991189699118GA11GENIChomozygous128678016
996991319699135GGAG14GENIChomozygous128678017
996997879699788AG44GENIChomozygous117243442
996998419699842GA47GENIChomozygous117243443
997002589700260GT7GENICheterozygous128678018
997020559702056CT44GENIChomozygous117243445
997022649702265CT46GENIChomozygous117243446