chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224874539224874540TC31GENIChomozygous108556253
1224874566224874567TC27GENIChomozygous108556254
1224874997224874998GT25GENICpossibly homozygous108556255
1224875042224875043GA8GENICpossibly homozygous108556256
1224875195224875196AG30GENIChomozygous108556258
1224876291224876292GA30GENIChomozygous108556259
1224877918224877919TC31GENIChomozygous108556260
1224878076224878077AG32GENIChomozygous108556261
1224878084224878085GA31GENIChomozygous108556262
1224878292224878293GA51GENIChomozygous108556263
1224880204224880205TC40GENIChomozygous108556264
1224881026224881027AG48GENIChomozygous108556265
1224881341224881342TC36GENIChomozygous108556266
1224882059224882060GA54GENIChomozygous108556267