| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128098254-128098537 | Common:2; Rare:59 | ||||
| chr9:128160018-128160479 | Common:2; Rare:109 | ||||
| chr9:128191448-128191673 | Rare:65 | ||||
| chr9:128191750-128191805 | Common:1; Rare:15 | ||||
| chr9:128191806-128191942 | Rare:36 | ||||
| chr9:128275267-128275370 | Common:1; Rare:22 | ||||
| chr9:128275914-128276302 | Common:5; Rare:172 | ||||
| chr9:128322376-128322621 | Common:1; Rare:82 | ||||
| chr9:128322729-128322870 | Common:2; Rare:55; Clinvar (benign):5 | ||||
| chr9:128340427-128340695 | Common:2; Rare:84 | ||||
| chr9:128371213-128371414 | Rare:80 | ||||
| chr9:128552408-128552597 | Rare:73; Clinvar:1 | ||||
| chr9:128656652-128656996 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:128724090-128724467 | Common:2; Rare:125 | ||||
| chr9:128771860-128772051 | Common:1; Rare:55 |