chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224874539224874540TC18GENIChomozygous108556253
1224874566224874567TC16GENIChomozygous108556254
1224874997224874998GT13GENIChomozygous108556255
1224875195224875196AG18GENIChomozygous108556258
1224876291224876292GA13GENIChomozygous108556259
1224877812224877813GA7GENIChomozygous125439394
1224877918224877919TC13GENIChomozygous108556260
1224878076224878077AG10GENIChomozygous108556261
1224878084224878085GA8GENIChomozygous108556262
1224878292224878293GA19GENIChomozygous108556263
1224880204224880205TC14GENIChomozygous108556264
1224881026224881027AG25GENIChomozygous108556265
1224881341224881342TC10GENICheterozygous108556266
1224882059224882060GA17GENIChomozygous108556267