chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263922828263922829GA18GENIChomozygous108634405
1263924243263924244AG16GENIChomozygous108634409
1263924770263924771TC23GENIChomozygous108634411
1263924809263924810TC19GENIChomozygous108634413
1263924813263924814TC22GENIChomozygous108634415
1263925145263925146TC36GENIChomozygous108634417
1263925452263925453TC33GENIChomozygous108634419
1263925612263925613AC27GENIChomozygous109217554
1263925806263925807TC26GENIChomozygous109217555
1263926884263926885TC25GENIChomozygous108634431
1263927944263927945AC23GENIChomozygous109217557
1263928068263928069TC32GENIChomozygous108634462
1263928425263928426GA41GENIChomozygous109217559
1263929904263929905AG36GENIChomozygous108634486
1263931239263931240TC21GENIChomozygous108634492
1263935971263935972TC15GENIChomozygous108634528
1263939384263939385CG26GENIChomozygous109217561
1263939942263939943CT33GENIChomozygous109217563
1263942843263942844AG20GENIChomozygous109217571
1263944464263944465AC13GENIChomozygous108634550
1263946663263946664GA31GENIChomozygous108634556
1263946683263946684TG33GENIChomozygous109217585
1263946701263946702GA35GENIChomozygous108634560
1263949168263949169GA13GENIChomozygous108634568
1263949689263949690AG18GENIChomozygous108634570
1263951728263951729TC14GENIChomozygous108634575
1263952407263952408TG13GENIChomozygous108634581
1263952897263952898CT27GENIChomozygous108634583
1263953846263953847CT14GENIChomozygous109217587
1263957815263957816GA19GENIChomozygous109217593
1263957918263957919CT18GENIChomozygous108782888
1263958764263958765TC23GENIChomozygous108634605
1263959038263959039CA25GENIChomozygous108782891