| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:133356452-133356618 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr9:133375965-133376349 | Common:3; Rare:140 | ||||
| chr9:133417862-133418319 | Common:5; Rare:129 | ||||
| chr9:134135320-134135403 | Common:1; Rare:17 | ||||
| chr9:134641555-134641845 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:136118803-136119041 | Common:4; Rare:101 | ||||
| chr9:136410603-136410697 | Common:1; Rare:51 | ||||
| chr9:136662707-136662955 | Common:1; Rare:61 | ||||
| chr9:136741985-136742082 | Rare:31 | ||||
| chr9:136746032-136746170 | Common:1; Rare:34 | ||||
| chr9:136746187-136746458 | Common:2; Rare:41 | ||||
| chr9:136799040-136799354 | Common:3; Rare:98 | ||||
| chr9:136799367-136799404 | Rare:7 | ||||
| chr9:136800134-136800489 | Common:5; Rare:106 | ||||
| chr9:136805169-136805456 | Common:1; Rare:84 |