| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20684078-20684292 | Common:3; Rare:85 | ||||
| chr9:21031438-21031560 | Common:2; Rare:45 | ||||
| chr9:21031586-21031691 | Common:1; Rare:45 | ||||
| chr9:21802461-21802700 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21975113-21975328 | Common:2; Rare:54; Clinvar (benign):1 | ||||
| chr9:21994344-21994575 | Rare:73; Clinvar:1; Clinvar (benign):4 | ||||
| chr9:22009211-22009478 | Common:1; Rare:87 | ||||
| chr9:23826294-23826482 | Common:1; Rare:77 | ||||
| chr9:26892331-26892545 | Rare:103 | ||||
| chr9:26892594-26892887 | Common:2; Rare:131 | ||||
| chr9:26947018-26947299 | Common:1; Rare:103 | ||||
| chr9:26956295-26956497 | Common:2; Rare:74 | ||||
| chr9:27573402-27573529 | Common:6; Rare:68 | ||||
| chr9:27573723-27573855 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384506-32384732 | Common:1; Rare:85 |