| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128191666-128191804 | Common:2; Rare:32 | ||||
| chr9:128191806-128191832 | Rare:5 | ||||
| chr9:128275929-128276302 | Common:5; Rare:171 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322739-128322912 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:128371220-128371398 | Rare:68 | ||||
| chr9:128455941-128456169 | Common:1; Rare:65 | ||||
| chr9:128504588-128504793 | Rare:94; Clinvar:5 | ||||
| chr9:128552394-128552681 | Rare:109; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:128724090-128724464 | Common:2; Rare:123 | ||||
| chr9:128787090-128787341 | Common:4; Rare:80 | ||||
| chr9:128881901-128882240 | Common:2; Rare:117 | ||||
| chr9:128882545-128882634 | Common:1; Rare:18 | ||||
| chr9:128921964-128922331 | Common:1; Rare:80 | ||||
| chr9:128947593-128947735 | Common:1; Rare:64; Clinvar:4; Clinvar (benign):1 |