| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128484723-128485006 | Common:2; Rare:72 | ||||
| chr9:128681732-128681771 | Rare:8 | ||||
| chr9:128684421-128684537 | Rare:22 | ||||
| chr9:128693656-128693977 | Rare:80; Clinvar:1 | ||||
| chr9:128945779-128946139 | Rare:109; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr9:129176701-129176975 | Common:2; Rare:94 | ||||
| chr9:129177334-129177477 | Common:1; Rare:58 | ||||
| chr9:129333745-129333933 | Common:1; Rare:31 | ||||
| chr9:129339743-129339875 | Common:2; Rare:39 | ||||
| chr9:129490586-129490850 | Rare:54 | ||||
| chr9:129497691-129498040 | Common:2; Rare:70 | ||||
| chr9:129828252-129828322 | Common:1; Rare:21 | ||||
| chr9:130712931-130713049 | Common:1; Rare:43 | ||||
| chr9:131194939-131195186 | Rare:42 | ||||
| chr9:131452269-131452363 | Common:3; Rare:18 |