chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147455742147455743AC15GENIChomozygous112874406
4147455975147455976TC22GENIChomozygous112874407
4147457347147457348GA24GENIChomozygous112874408
4147457890147457891TC22GENIChomozygous112874409
4147458012147458013AG27GENIChomozygous112874410
4147458232147458233AG23GENIChomozygous112874411
4147458283147458284GA19GENICheterozygous112874412
4147458462147458463GA31GENIChomozygous112874413
4147459153147459154GC23GENIChomozygous112874414
4147459200147459201TC22GENIChomozygous112874415
4147459661147459662AG23GENIChomozygous112874417
4147460042147460043CT19GENIChomozygous112874418
4147460443147460444CT19GENIChomozygous112874419
4147460444147460445AC20GENIChomozygous112874420
4147460462147460463AC21GENIChomozygous112874421
4147460476147460477TC24GENIChomozygous112874422
4147466098147466099AC21GENIChomozygous112874423
4147466211147466212TG26GENIChomozygous112874424
4147466911147466912CT19GENIChomozygous112874425
4147468254147468255TG28GENIChomozygous112874426
4147469880147469881GC17GENIChomozygous112874427
4147471863147471864TC22GENIChomozygous112874431
4147474252147474253GA18GENIChomozygous112874433
4147475400147475401TG29GENIChomozygous112874434
4147475894147475895TC33GENIChomozygous112874435
4147476213147476214CA36GENIChomozygous112874436
4147477451147477452AG22GENIChomozygous112874438
4147480102147480103GA29GENIChomozygous112874439
4147480283147480284AG23GENIChomozygous112874440
4147481614147481615AG13GENIChomozygous112874441
4147482328147482329GA21GENIChomozygous112874442
4147482393147482394GC33GENIChomozygous112874443
4147484658147484659AG20GENIChomozygous112874444
4147485156147485157GT26GENIChomozygous112874447
4147486712147486713GA30GENIChomozygous119281734
4147487224147487225CT26GENIChomozygous112874448
4147488001147488002GA18GENIChomozygous112874449
4147489044147489045CT20GENIChomozygous112874450
4147489302147489303CT16GENIChomozygous112874452
4147489604147489605GA11GENIChomozygous112874453