chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG20GENIChomozygous113347829
141297497912974980GA17GENIChomozygous113347831
141297572712975728TC22GENIChomozygous113347833
141297600712976008TC17GENIChomozygous113347835
141297603412976035AT15GENIChomozygous113347837
141297704912977050TC12GENIChomozygous113347839
141297778012977781GT27GENIChomozygous113347841
141297853412978535TC18GENIChomozygous113347843
141297897412978975AT26GENIChomozygous113347845
141298059712980598CT27GENIChomozygous113347847
141298061312980614GA35GENIChomozygous113347849
141298103212981033CA13GENIChomozygous113347851
141298248612982487TC23GENIChomozygous113347853
141298580612985807AG15GENIChomozygous113347855
141298595912985960TG25GENIChomozygous113347857
141298615112986152AG14GENIChomozygous113347859
141298676312986764AC11GENIChomozygous113347861
141298684212986843AC23GENIChomozygous113347863
141298761312987614TG25GENIChomozygous113347865
141298766312987664GA22GENIChomozygous113347867
141298792112987922AT21GENIChomozygous113347869
141298835612988357GC21GENIChomozygous113347871
141298866412988665CA15GENIChomozygous113347873
141298876812988769GA9GENIChomozygous113347875
141298877612988777AT10GENIChomozygous113347877
141298889712988898TG25GENIChomozygous113347879
141299108112991082CT22GENIChomozygous113347881
141299289412992895TC22GENIChomozygous113347883
141299411712994118TC13GENIChomozygous113347887
141299423612994237CG13GENIChomozygous113347889
141298173012981731AG21GENIChomozygous113574933
141298846512988466TG15GENIChomozygous113574934