chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124123558124123559CT27GENIChomozygous115164483
6124123942124123943CA29GENIChomozygous114976909
6124124140124124141AG18GENIChomozygous115164484
6124124837124124838CG18GENIChomozygous114976912
6124124864124124865TG15GENIChomozygous114976913
6124124883124124884TC16GENIChomozygous115164485
6124124919124124920CT16GENIChomozygous114976914
6124124921124124922AG15GENIChomozygous115164486
6124126112124126113AC30GENIChomozygous115164490
6124126121124126122GC37GENIChomozygous115164491
6124126837124126838CT24GENIChomozygous115164492
6124129210124129211CT30GENIChomozygous115164493
6124131352124131353AG43GENIChomozygous115164494
6124131360124131361TC42GENIChomozygous115164495
6124131420124131421CT50GENIChomozygous115164496
6124131431124131432AG49GENIChomozygous115164497
6124131438124131439GA50GENIChomozygous115164498
6124131580124131581AG37GENIChomozygous115164499
6124131761124131762TG35GENIChomozygous115164500
6124131763124131764AG36GENIChomozygous115164501
6124131853124131854GC41GENIChomozygous115164502
6124132268124132269GA34GENIChomozygous115164503
6124132439124132440TC29GENIChomozygous115164504
6124133329124133330TC38GENIChomozygous115164505
6124133456124133457AG42GENIChomozygous115164506
6124133460124133461TA41GENIChomozygous115164507
6124133729124133730TA46GENIChomozygous115164508
6124133747124133748AG44GENIChomozygous115164509
6124133945124133946TC30GENIChomozygous114976918
6124134123124134124CT23GENIChomozygous115164510
6124134463124134464GA21GENIChomozygous115164511
6124134926124134927GA25GENIChomozygous115164513
6124135005124135006CT17GENIChomozygous115164514
6124135049124135050AG16GENIChomozygous115164515
6124135598124135599CG45GENIChomozygous115164517