chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117460914117460915GT23GENIChomozygous958567885
8117462354117462355CT23GENIChomozygous958567886
8117463142117463143AG9GENIChomozygous958567887
8117463763117463764CT20GENIChomozygous958567888
8117464369117464370AG5GENIChomozygous958567889
8117464395117464396CG10GENIChomozygous958567890
8117464601117464602TC15GENIChomozygous958567891
8117464876117464877GA25GENIChomozygous958567892
8117466249117466250AC17GENIChomozygous958567893
8117466513117466514TC24GENIChomozygous958567894
8117467475117467476TG7GENIChomozygous958567895
8117467476117467477TG6GENIChomozygous958567896
8117468441117468442GA19GENIChomozygous958567897
8117469362117469363TC19GENIChomozygous958567898
8117470014117470015TC13GENIChomozygous958567899
8117471283117471284TC12GENIChomozygous958567900
8117471357117471358AT15GENIChomozygous958567901
8117475110117475111CA21GENIChomozygous958567902