chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105531479955314800GA20GENIChomozygous51652719
105531520155315202CT28GENIChomozygous51652721
105531551755315518AG25GENIChomozygous51652722
105531570755315708T-20GENIChomozygous51652726
105531587155315872AG25GENIChomozygous51652728
105531777555317776TA16GENIChomozygous51652730
105531782455317828CAGA----20GENIChomozygous51459395
105531860155318602CT22GENIChomozygous51459396
105531907955319080AT15GENIChomozygous51459397
105531935955319360GA13GENIChomozygous51889647
105531936355319364GGGA13GENIChomozygous51652732
105531990055319901GA22GENIChomozygous51652734
105532082055320821AG10GENIChomozygous51459398
105532282255322823AAAAGCAAAGCAACAT9GENIChomozygous51459400
105532395155323959TGTGTGTG--------8GENIChomozygous52800823
105532399755323998TC15GENIChomozygous51459402
105532422055324221AC11GENIChomozygous51459403
105532585855325859TC12GENIChomozygous51459404
105532628755326288AG14GENIChomozygous51459405
105532800355328004AG8GENIChomozygous51459407
105532911055329111GA13GENIChomozygous51459408
105532911255329113TC13GENIChomozygous52561646
105532941555329416AG18GENIChomozygous51459409
105533043855330439TC19GENIChomozygous51459410
105533059955330610TTTTGTTTTGT-----------10GENIChomozygous53148548
105533230155332302AAGAG12GENIChomozygous51459414
105533323355333234CT13GENIChomozygous51459415
105533354755333548CT17GENIChomozygous52561649
105533384555333846TA16GENIChomozygous53527576
105533384655333847TA16GENIChomozygous53527578
105533480655334807TG8GENIChomozygous52561652
105533510855335109G-13GENIChomozygous52561655
105533551955335520AT12GENIChomozygous51459417
105533555955335562TAT---12GENIChomozygous51459418