| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33025090-33025356 | Common:7; Rare:116 | ||||
| chr9:33076606-33076850 | Common:2; Rare:83 | ||||
| chr9:33264218-33264435 | Rare:95 | ||||
| chr9:33264718-33265148 | Rare:120 | ||||
| chr9:33290250-33290564 | Common:3; Rare:104 | ||||
| chr9:33473877-33474140 | Common:2; Rare:75 | ||||
| chr9:33816892-33817201 | Common:1; Rare:94 | ||||
| chr9:33817826-33817912 | Rare:18 | ||||
| chr9:34178775-34179153 | Common:1; Rare:92 | ||||
| chr9:34329310-34329612 | Common:1; Rare:82 | ||||
| chr9:34612059-34612238 | Common:9; Rare:68 | ||||
| chr9:34646579-34646714 | Rare:40; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:34665363-34665628 | Rare:84 | ||||
| chr9:35489922-35490153 | Common:3; Rare:65 | ||||
| chr9:35538499-35538651 | Common:1; Rare:21 |