| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132670401-132670511 | Rare:34 | ||||
| chr9:132878279-132878355 | Common:1; Rare:26 | ||||
| chr9:133030471-133030743 | Common:4; Rare:70 | ||||
| chr9:133336119-133336345 | Common:1; Rare:96 | ||||
| chr9:133348039-133348258 | Common:2; Rare:86 | ||||
| chr9:133356443-133356618 | Common:1; Rare:82; Clinvar (benign):2 | ||||
| chr9:133375999-133376370 | Common:1; Rare:133 | ||||
| chr9:133417939-133418110 | Common:2; Rare:45 | ||||
| chr9:136410609-136410680 | Rare:36 | ||||
| chr9:136662738-136662937 | Common:1; Rare:49 | ||||
| chr9:136746010-136746172 | Common:1; Rare:38 | ||||
| chr9:136800134-136800392 | Common:5; Rare:81 | ||||
| chr9:137086832-137087136 | Common:1; Rare:131; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137188541-137188733 | Common:2; Rare:94 | ||||
| chr9:137205646-137205739 | Rare:39 |