| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:123097533-123097786 | Rare:42 | ||||
| chr9:123549473-123549560 | Rare:12 | ||||
| chr9:124216811-124216985 | Common:1; Rare:36 | ||||
| chr9:124353927-124354251 | Common:4; Rare:69 | ||||
| chr9:124354259-124354412 | Rare:24 | ||||
| chr9:124354750-124355002 | Common:1; Rare:56 | ||||
| chr9:124355209-124355486 | Common:2; Rare:65 | ||||
| chr9:124357423-124357794 | Common:1; Rare:71 | ||||
| chr9:124497301-124497589 | Common:1; Rare:49 | ||||
| chr9:124498355-124498477 | Common:1; Rare:23 | ||||
| chr9:124503337-124503574 | Common:1; Rare:58; Clinvar (pathogenic):1 | ||||
| chr9:124504941-124505118 | Common:3; Rare:57 | ||||
| chr9:124505430-124505829 | Common:3; Rare:89 | ||||
| chr9:124508042-124508292 | Rare:55 | ||||
| chr9:124658319-124658443 | Rare:22 |