chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7140273278140273279CG21INTERGENIChomozygous54153300
7140273552140273553AT14INTERGENIChomozygous54261537
7140273785140273786GT10INTERGENIChomozygous54261540
7140273791140273793GT--9INTERGENIChomozygous56444060
7140275490140275491TA18INTERGENIChomozygous54153308
7140275899140275910ATGAACACAAC-----------10INTERGENIChomozygous54261552
7140277468140277469AG14INTERGENIChomozygous54153316
7140277611140277612TC11INTERGENIChomozygous54153318
7140277737140277738TG21INTERGENIChomozygous54261558
7140278815140278816CCT11INTERGENIChomozygous54261564
7140279743140279744TC15INTERGENIChomozygous54153343
7140280355140280356CT18INTERGENIChomozygous54261567
7140280461140280462GA14INTERGENIChomozygous54261569
7140280519140280520CT23INTERGENIChomozygous54261572
7140282418140282419GC9INTERGENIChomozygous54153351
7140282423140282424GA10INTERGENIChomozygous54153353
7140284859140284860TC18INTERGENIChomozygous54261584
7140284967140284968CT18INTERGENIChomozygous54261587
7140285340140285341CT14INTERGENIChomozygous54261590
7140285759140285760CT14INTERGENIChomozygous54261593
7140287639140287640TC11INTERGENIChomozygous54261596
7140288132140288133GA18INTERGENICheterozygous56444062
7140288145140288146TG19INTERGENICheterozygous56444064
7140288522140288552CTATGGCAGAAGGGACATATGGCTCCACTG------------------------------6INTERGENIChomozygous56444066
7140289329140289330GA18INTERGENIChomozygous54261626
7140289527140289528CT10INTERGENIChomozygous54261629
7140290449140290450AG18INTERGENIChomozygous54153378
7140291159140291160TC8INTERGENIChomozygous54153380
7140291492140291493CG16INTERGENIChomozygous54261632
7140291714140291716GG--9INTERGENIChomozygous54261635