| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:29213430-29213579 | Rare:53 | ||||
| chr9:29214185-29214336 | Common:2; Rare:45 | ||||
| chr9:32550876-32551187 | Common:1; Rare:127; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33818759-33818784 | Rare:1 | ||||
| chr9:33818796-33818883 | Rare:15 | ||||
| chr9:34380790-34380900 | Common:1; Rare:36 | ||||
| chr9:34552021-34552295 | Common:1; Rare:87 | ||||
| chr9:34557594-34557904 | Rare:80 | ||||
| chr9:34701480-34701521 | Rare:10 | ||||
| chr9:35604014-35604402 | Common:3; Rare:103 | ||||
| chr9:36352590-36352774 | Common:1; Rare:44 | ||||
| chr9:36352996-36353246 | Rare:66 | ||||
| chr9:39464482-39464657 | Common:1; Rare:41 | ||||
| chr9:39809312-39809498 | Common:4; Rare:16 | ||||
| chr9:40991948-40992368 | Common:7; Rare:33 |