chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224874539224874540TC47GENIChomozygous108556253
1224874566224874567TC47GENIChomozygous108556254
1224874997224874998GT24GENICheterozygous108556255
1224875042224875043GA21GENICpossibly homozygous108556256
1224875072224875073GA28GENICheterozygous108556257
1224875195224875196AG46GENIChomozygous108556258
1224876291224876292GA38GENIChomozygous108556259
1224877918224877919TC41GENIChomozygous108556260
1224878076224878077AG41GENIChomozygous108556261
1224878084224878085GA40GENIChomozygous108556262
1224878292224878293GA55GENIChomozygous108556263
1224880204224880205TC29GENIChomozygous108556264
1224881026224881027AG58GENIChomozygous108556265
1224881341224881342TC48GENIChomozygous108556266
1224882059224882060GA50GENIChomozygous108556267