chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG12GENIChomozygous113347829
141297497912974980GA10GENIChomozygous113347831
141297572712975728TC22GENIChomozygous113347833
141297600712976008TC17GENIChomozygous113347835
141297603412976035AT19GENIChomozygous113347837
141297778012977781GT18GENIChomozygous113347841
141297853412978535TC15GENIChomozygous113347843
141297897412978975AT15GENIChomozygous113347845
141298059712980598CT7GENIChomozygous113347847
141298061312980614GA8GENIChomozygous113347849
141298103212981033CA13GENIChomozygous113347851
141298248612982487TC12GENIChomozygous113347853
141298580612985807AG14GENIChomozygous113347855
141298595912985960TG14GENIChomozygous113347857
141298615112986152AG12GENIChomozygous113347859
141298676312986764AC8GENIChomozygous113347861
141298684212986843AC11GENIChomozygous113347863
141298761312987614TG18GENIChomozygous113347865
141298766312987664GA27GENIChomozygous113347867
141298792112987922AT10GENIChomozygous113347869
141298835612988357GC23GENIChomozygous113347871
141298866412988665CA15GENIChomozygous113347873
141298876812988769GA13GENIChomozygous113347875
141298877612988777AT5GENIChomozygous113347877
141298889712988898TG6GENIChomozygous113347879
141299267112992672GA3GENICheterozygous123859688
141299289412992895TC11GENIChomozygous113347883
141299407112994072GA10GENIChomozygous113347885
141299473212994733TG12GENIChomozygous113347891