chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140522364140522365AG29GENIChomozygous108257671
1140523045140523045GC28GENIChomozygous127438369
1140523047140523047T28GENIChomozygous127438370
1140525367140525367CACCT11GENIChomozygous127438374
1140526614140526615TC23GENIChomozygous108257685
1140527350140527351TG28GENIChomozygous108257687
1140529184140529185CA28GENIChomozygous109144205
1140525551140525552CT17GENIChomozygous109144192
1140525930140525931AG23GENIChomozygous109144198
1140526889140526890CT18GENIChomozygous109144200
1140527335140527336GA27GENIChomozygous109144202
1140527743140527744GA21GENIChomozygous109144204
1140529227140529228AG28GENIChomozygous109144207
1140529290140529290T23GENIChomozygous130823353
1140529336140529337CT23GENIChomozygous109144209
1140529888140529889TC25GENIChomozygous109144211
1140530270140530271AG19GENIChomozygous109144213
1140530613140530614CT11GENIChomozygous109144215
1140530686140530687CG9GENIChomozygous109144217
1140530702140530703GA8GENIChomozygous109144219
1140530754140530754TAT18GENIChomozygous130823354
1140531266140531266CAAGGGAGT15GENIChomozygous130823355
1140531295140531306AGACCACACTT16GENIChomozygous130823356
1140531795140531798CCT31GENIChomozygous130823357
1140533130140533142AGATTTCTCTCG15GENIChomozygous130823358
1140534502140534503C7GENIChomozygous130823359
1140534506140534507A7GENIChomozygous127438375
1140535366140535367AT19GENIChomozygous109144229
1140532859140532860CT23GENIChomozygous109144221
1140533188140533189AG16GENIChomozygous108257697
1140533256140533257CA15GENIChomozygous109144223
1140534186140534187TC15GENIChomozygous109144225
1140534467140534468TC14GENIChomozygous109144227
1140529297140529298AT23GENIChomozygous120486519
1140530808140530809AT26GENIChomozygous120486520
1140530813140530814TG26GENIChomozygous120486521
1140531559140531560TA21GENIChomozygous120486522
1140531560140531561CT21GENIChomozygous120486523
1140530630140530631AG12GENIChomozygous120728922