chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4147458232147458233AG12GENIChomozygous112874411
4147458283147458284GA5GENIChomozygous112874412
4147458462147458463GA17GENIChomozygous112874413
4147459153147459154GC13GENIChomozygous112874414
4147459200147459201TC16GENIChomozygous112874415
4147459382147459383AT9GENICheterozygous112874416
4147459661147459662AG13GENIChomozygous112874417
4147460462147460463AC4GENIChomozygous112874421
4147460476147460477TC11GENIChomozygous112874422
4147466098147466099AC20GENIChomozygous112874423
4147466211147466212TG7GENIChomozygous112874424
4147466911147466912CT25GENIChomozygous112874425
4147467751147467752GC8GENIChomozygous126025081
4147468254147468255TG10GENIChomozygous112874426
4147469880147469881GC28GENIChomozygous112874427
4147471863147471864TC11GENIChomozygous112874431
4147473504147473505TA13GENIChomozygous112874432
4147474252147474253GA16GENIChomozygous112874433
4147475400147475401TG19GENIChomozygous112874434
4147475894147475895TC22GENIChomozygous112874435
4147476213147476214CA19GENIChomozygous112874436
4147477451147477452AG21GENIChomozygous112874438
4147480102147480103GA17GENIChomozygous112874439
4147480283147480284AG10GENIChomozygous112874440
4147481614147481615AG16GENIChomozygous112874441
4147482328147482329GA21GENIChomozygous112874442
4147482393147482394GC20GENIChomozygous112874443
4147484658147484659AG20GENIChomozygous112874444
4147485156147485157GT18GENIChomozygous112874447
4147487224147487225CT6GENIChomozygous112874448
4147488001147488002GA5GENIChomozygous112874449
4147489044147489045CT20GENIChomozygous112874450
4147489130147489131TA5GENIChomozygous112874451
4147489604147489605GA8GENIChomozygous112874453