chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
499101619910162CT17GENIChomozygous56744406
499103619910362CT35GENIChomozygous56744407
499105469910547TC29GENIChomozygous56744408
499114129911413TG27GENIChomozygous56744409
499118959911896GA25GENIChomozygous56744410
499123179912318AACACTAC43GENIChomozygous56744411
499129469912947AG36GENIChomozygous56744412
499133459913346AG23GENIChomozygous56744413
499133619913362TG27GENIChomozygous56744414
499135509913551AG26GENIChomozygous56744415
499138029913803TG31GENIChomozygous56744416
499140289914029CCT11GENIChomozygous56744417
499143599914360TC19GENIChomozygous56744418
499155999915615GAAACAAACAAACAAA----------------33GENIChomozygous56744424
499164359916436GA28GENIChomozygous56744426
499187079918708AT23GENIChomozygous56744427
499188319918832AT18GENIChomozygous56744428
499190299919030GA22GENIChomozygous56744429
499190669919067AG17GENIChomozygous56744430
499198529919853GA42GENIChomozygous56744431
499200689920069AAAACAACAACAAC18GENICheterozygous56744432
499214169921417AAG19GENIChomozygous56744434
499221729922173TC14GENIChomozygous56744435
499221949922195TTA2GENIChomozygous56744436
499222759922276CA21GENIChomozygous56744437
499225899922590GA4GENIChomozygous56744438
499200689920069AAAACAACAACAACAACAACAAC18GENICpossibly homozygous58326931
499200689920069AAAACAACAACAACAACAACAACAAC18GENICheterozygous58326932
499208079920833GTGTGTGTGTGTGTGTGTGTGTGTGT--------------------------8GENIChomozygous58274293