chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2045424054542406AG11GENIChomozygous125175858
2045424134542414TC12GENIChomozygous125175859
2045429544542955TC12GENIChomozygous125175860
2045449734544974GA35GENIChomozygous125175861
2045454384545439GA15GENIChomozygous125175862
2045455684545569TG4GENICheterozygous125175863
2045455754545576AT5GENIChomozygous125175864
2045462494546250TC25GENIChomozygous125175865
2045472704547271CT21GENIChomozygous125175866
2045482304548231GT8GENICheterozygous125175867
2045482314548232GT8GENICheterozygous125175868
2045488394548840CA13GENIChomozygous125175869
2045490624549063CA24GENIChomozygous125175870
2045504624550463CG14GENIChomozygous125175871
2045509694550970TC11GENICheterozygous125175872
2045513954551396TC34GENIChomozygous125175873
2045514934551494AG27GENICheterozygous125175874
2045515134551514TA10GENICheterozygous125175875
2045518094551810TG7GENIChomozygous125175876
2045520744552075GT19GENIChomozygous125175877
2045590254559026CT12GENIChomozygous125175878
2045591854559186CT18GENIChomozygous125175879
2045592954559296GA18GENIChomozygous125175880
2045596394559640CT13GENIChomozygous125175881