chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140522364140522365AG37GENIChomozygous108257671
1140525551140525552CT35GENICpossibly homozygous109144192
1140525930140525931AG25GENIChomozygous109144198
1140526614140526615TC30GENIChomozygous108257685
1140526889140526890CT27GENIChomozygous109144200
1140527335140527336GA37GENIChomozygous109144202
1140527350140527351TG36GENIChomozygous108257687
1140527743140527744GA19GENIChomozygous109144204
1140529184140529185CA17GENIChomozygous109144205
1140529227140529228AG21GENIChomozygous109144207
1140529297140529298AT10GENIChomozygous120486519
1140529336140529337CT11GENIChomozygous109144209
1140529888140529889TC32GENIChomozygous109144211
1140530270140530271AG24GENIChomozygous109144213
1140530808140530809AT10GENIChomozygous120486520
1140530813140530814TG9GENIChomozygous120486521
1140531559140531560TA23GENIChomozygous120486522
1140531560140531561CT22GENIChomozygous120486523
1140532859140532860CT25GENIChomozygous109144221
1140533188140533189AG13GENIChomozygous108257697
1140533256140533257CA16GENIChomozygous109144223
1140534186140534187TC19GENIChomozygous109144225
1140535366140535367AT33GENIChomozygous109144229