| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131630302-131630698 | Common:1; Rare:72 | ||||
| chr9:131658421-131658589 | Common:2; Rare:25 | ||||
| chr9:131677455-131677745 | Rare:43 | ||||
| chr9:132662338-132662414 | Rare:27 | ||||
| chr9:132662578-132662818 | Common:2; Rare:74 | ||||
| chr9:133126326-133126484 | Common:1; Rare:22 | ||||
| chr9:133200069-133200240 | Common:1; Rare:45 | ||||
| chr9:133656339-133656473 | Common:1; Rare:39 | ||||
| chr9:134766204-134766498 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:134766681-134766817 | Common:3; Rare:25 | ||||
| chr9:135960040-135960191 | Common:2; Rare:32 | ||||
| chr9:136094168-136094253 | Rare:21 | ||||
| chr9:136644469-136644579 | Common:1; Rare:25 | ||||
| chr9:136669068-136669266 | Rare:27 | ||||
| chr9:136725078-136725405 | Rare:72 |