chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245699988245699989C17GENIChomozygous127500391
1245700002245700004TT14GENIChomozygous127500392
1245700004245700005TG13GENIChomozygous120512565
1245700026245700027C7GENIChomozygous127500393
1245700036245700037G20GENIChomozygous127500394
1245700064245700064G16GENIChomozygous127500395
1245700068245700068G16GENIChomozygous127500396
1245700078245700079C17GENIChomozygous127500397
1245700080245700081C16GENIChomozygous127500398
1245700098245700104GAGGAA14GENIChomozygous127500399
1245700130245700131T11GENIChomozygous127500400
1245700136245700137A11GENIChomozygous127500401
1245700147245700148G10GENIChomozygous127500402
1245700165245700167AG9GENIChomozygous127500403
1245700170245700170CCA9GENIChomozygous127500404
1245700176245700177A8GENIChomozygous127500405
1245700199245700200AC4GENIChomozygous121206799
1245700200245700201TA3GENIChomozygous120907052
1245700192245700193A5GENIChomozygous129845809
1245700207245700209TG3GENIChomozygous129845810
1245700322245700322C21GENIChomozygous130521282
1245700341245700342C19GENIChomozygous127500406
1245700342245700343GA19GENIChomozygous121206802
1245700358245700359T19GENIChomozygous127500407
1245700369245700369C16GENIChomozygous127500408
1245700371245700371A14GENIChomozygous127500409
1245700376245700377T14GENIChomozygous127500410
1245700379245700380A14GENIChomozygous127500411
1245700387245700388AG14GENIChomozygous121206808
1245700394245700395C14GENIChomozygous127500412
1245700402245700403AC12GENIChomozygous109208801
1245700406245700406G12GENIChomozygous127500413
1245700415245700416A9GENIChomozygous127500414
1245700428245700429GA8GENIChomozygous108600267
1245700434245700435A7GENIChomozygous127500415
1245700453245700454CA2GENIChomozygous108600268
1245700456245700457A2GENIChomozygous127500416
1245717837245717838T4GENIChomozygous127500421
1245728659245728661GA32GENICheterozygous132541387