chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140887405140887406GC40GENIChomozygous978862385
4140887526140887527AG23GENIChomozygous978862386
4140894149140894150GA50GENIChomozygous978862387
4140894483140894484TC23GENIChomozygous978862388
4140894658140894659GC43GENIChomozygous978862389
4140896988140896989GA57GENIChomozygous978862390
4140899328140899329GA60GENIChomozygous978862391
4140902715140902716TC16GENIChomozygous978862392
4140902957140902958AG27GENIChomozygous978862393
4140903807140903808CT15GENIChomozygous978862394
4140906395140906396AG40GENIChomozygous978862395
4140908274140908275TG33GENIChomozygous978862396
4140908994140908995GC26GENIChomozygous978862397
4140909042140909043GA35GENIChomozygous978862398
4140909059140909060CA36GENIChomozygous978862399
4140909109140909110GA27GENIChomozygous978862400
4140909129140909130CT25GENIChomozygous978862401
4140909170140909171GA30GENIChomozygous978862402
4140909196140909197CT33GENIChomozygous978862403
4140909244140909245GT36GENIChomozygous978862404
4140909248140909249TA34GENIChomozygous978862405
4140909269140909270GA26GENIChomozygous978862406
4140909286140909287GC23GENIChomozygous978862407
4140913522140913523CT26GENIChomozygous978862408
4140916630140916631TG24GENIChomozygous978862409
4140916631140916632CA23GENIChomozygous978862410
4140916937140916938GA51GENIChomozygous978862411