chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG27GENIChomozygous113347829
141297497912974980GA24GENIChomozygous113347831
141297572712975728TC30GENIChomozygous113347833
141297600712976008TC44GENIChomozygous113347835
141297603412976035AT48GENIChomozygous113347837
141297709012977091GA5GENIChomozygous113718108
141297778012977781GT21GENIChomozygous113347841
141297853412978535TC36GENIChomozygous113347843
141297897412978975AT27GENIChomozygous113347845
141298059712980598CT23GENIChomozygous113347847
141298061312980614GA25GENIChomozygous113347849
141298103212981033CA25GENIChomozygous113347851
141298248612982487TC43GENIChomozygous113347853
141298580612985807AG35GENIChomozygous113347855
141298595912985960TG26GENIChomozygous113347857
141298615112986152AG23GENIChomozygous113347859
141298676312986764AC10GENIChomozygous113347861
141298684212986843AC37GENIChomozygous113347863
141298761312987614TG26GENIChomozygous113347865
141298766312987664GA29GENIChomozygous113347867
141298792112987922AT19GENIChomozygous113347869
141298835612988357GC21GENIChomozygous113347871
141298866412988665CA29GENIChomozygous113347873
141298876812988769GA29GENIChomozygous113347875
141298877612988777AT29GENIChomozygous113347877
141298889712988898TG27GENIChomozygous113347879
141299108112991082CT23GENIChomozygous113347881
141298846512988466TG17GENIChomozygous113574934
141299289412992895TC41GENIChomozygous113347883
141299407112994072GA24GENIChomozygous113347885
141299411712994118TC21GENIChomozygous113347887
141299423612994237CG22GENIChomozygous113347889
141299473212994733TG38GENIChomozygous113347891