| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112175295-112175445 | Common:2; Rare:38 | ||||
| chr9:112379811-112380140 | Common:3; Rare:133 | ||||
| chr9:112718033-112718397 | Common:2; Rare:88 | ||||
| chr9:112890781-112891068 | Common:3; Rare:75 | ||||
| chr9:113221217-113221598 | Common:1; Rare:124 | ||||
| chr9:113275529-113275685 | Common:1; Rare:57; Clinvar (pathogenic):1 | ||||
| chr9:113580719-113580943 | Common:3; Rare:37 | ||||
| chr9:114387964-114388104 | Common:1; Rare:47 | ||||
| chr9:114587411-114587915 | Common:4; Rare:175 | ||||
| chr9:114930223-114930320 | Rare:32 | ||||
| chr9:114930470-114930686 | Common:4; Rare:54 | ||||
| chr9:120793367-120793507 | Rare:50 | ||||
| chr9:120842917-120843075 | Common:1; Rare:49 | ||||
| chr9:120876582-120876690 | Rare:28 | ||||
| chr9:120877157-120877509 | Common:3; Rare:122 |