chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134854064134854065AG15GENIChomozygous126204460
5134854533134854534GA14GENIChomozygous126204461
5134854570134854571TG16GENIChomozygous126204462
5134854865134854866AG13GENIChomozygous126204463
5134855560134855561CT19GENIChomozygous126204464
5134857330134857331TC20GENIChomozygous126204465
5134857422134857423AG17GENIChomozygous126204466
5134861805134861806TC22GENIChomozygous126204467
5134862391134862392TC10GENIChomozygous126204468
5134863287134863288TC9GENIChomozygous126204469
5134863646134863647CG15GENIChomozygous126204470
5134863780134863781TC23GENIChomozygous126204471
5134864051134864052CT23GENICpossibly homozygous126204472
5134864794134864795CT18GENIChomozygous126204473
5134865173134865174GA24GENIChomozygous126204474
5134865396134865397TC16GENIChomozygous126204475
5134865707134865708GA13GENIChomozygous126204476
5134865960134865961GC22GENIChomozygous126204477
5134867037134867038TC27GENIChomozygous126204478
5134867517134867518TC13GENIChomozygous126204479
5134867531134867532GA15GENIChomozygous126204480
5134868227134868228TC20GENIChomozygous126204481
5134868243134868244AC17GENIChomozygous126204482
5134869388134869389TC13GENICheterozygous126204483
5134869613134869614GA16GENIChomozygous126204484
5134863875134863876GA4GENICheterozygous126260597
5134863876134863877TC5GENICheterozygous126260598
5134863883134863884AG9GENIChomozygous126260599