chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1250557300250557301CT10GENIChomozygous61630790
1250557585250557586TTCTC7GENIChomozygous61630791
1250557912250557913TC12GENIChomozygous61630792
1250559472250559473GA10GENIChomozygous61630795
1250560170250560171CT10GENIChomozygous61630797
1250561529250561530CA22GENIChomozygous61156400
1250561678250561679CA13GENIChomozygous61156401
1250561827250561828CT19GENIChomozygous61156402
1250561839250561840TC20GENIChomozygous61156403
1250561967250561968TC13GENIChomozygous61156404
1250562013250562014A-7GENIChomozygous61684048
1250562667250562668TG9GENIChomozygous61156405
1250563105250563106TA13GENIChomozygous61156406
1250564487250564488GC13GENIChomozygous61156411
1250564857250564858CT12GENIChomozygous61156412
1250565239250565240GA12GENIChomozygous61156413
1250565326250565327AG11GENIChomozygous61156415
1250566460250566461GA8GENIChomozygous61156416
1250566673250566674GA10GENIChomozygous61156417