| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15552832-15552904 | Common:1; Rare:26 | ||||
| chr9:16870719-16870820 | Rare:44 | ||||
| chr9:17134896-17135197 | Common:1; Rare:144 | ||||
| chr9:19102863-19103051 | Common:2; Rare:80 | ||||
| chr9:19127455-19127635 | Common:3; Rare:57 | ||||
| chr9:19380188-19380349 | Common:4; Rare:77 | ||||
| chr9:20684096-20684289 | Common:3; Rare:78 | ||||
| chr9:21802515-21802696 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994229-21994293 | Rare:29; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr9:21994312-21994755 | Common:2; Rare:128; Clinvar:3; Clinvar (benign):6 | ||||
| chr9:22009295-22009482 | Common:1; Rare:57 | ||||
| chr9:23826309-23826545 | Common:1; Rare:94 | ||||
| chr9:26892737-26892895 | Common:1; Rare:78 | ||||
| chr9:26947107-26947566 | Common:2; Rare:155 | ||||
| chr9:26956260-26956459 | Common:2; Rare:73 |