chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141297492712974928AG24GENIChomozygous113347829
141297519412975195AG15GENIChomozygous113718106
141297572712975728TC33GENIChomozygous113347833
141297600712976008TC28GENIChomozygous113347835
141297603412976035AT30GENIChomozygous113347837
141297704912977050TC15GENIChomozygous113347839
141297709012977091GA5GENIChomozygous113718108
141297859112978592CT4GENIChomozygous113718110
141297897412978975AT23GENIChomozygous113347845
141297912512979126GT20GENIChomozygous113718112
141298061312980614GA24GENIChomozygous113347849
141298096712980968GA22GENIChomozygous113718114
141298248612982487TC33GENIChomozygous113347853
141298580612985807AG30GENIChomozygous113347855
141298595912985960TG30GENIChomozygous113347857
141298767512987676AG34GENIChomozygous113718116
141298792112987922AT16GENIChomozygous113347869
141298835612988357GC22GENIChomozygous113347871
141298866412988665CA26GENIChomozygous113347873
141298876812988769GA23GENIChomozygous113347875
141298877612988777AT22GENIChomozygous113347877
141298885412988855TG26GENIChomozygous113656706
141298889712988898TG30GENIChomozygous113347879
141298932912989330GA19GENIChomozygous113718118
141298998812989989AT22GENIChomozygous113718120
141299016312990164TA22GENIChomozygous113718122
141299411712994118TC26GENIChomozygous113347887
141299473212994733TG38GENIChomozygous113347891