| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127450729-127451062 | Common:3; Rare:75 | ||||
| chr9:127451261-127451562 | Common:3; Rare:124; Clinvar (benign):1 | ||||
| chr9:127612018-127612344 | Common:1; Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127762416-127762557 | Common:1; Rare:27 | ||||
| chr9:127854323-127854414 | Common:2; Rare:20; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:127854610-127854877 | Rare:55; Clinvar:5 | ||||
| chr9:127877661-127877803 | Rare:28 | ||||
| chr9:127937816-127937923 | Common:1; Rare:31; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128191474-128191651 | Rare:53 | ||||
| chr9:128191745-128191857 | Common:1; Rare:29 | ||||
| chr9:128275903-128276294 | Common:4; Rare:172 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322729-128322906 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128340425-128340695 | Common:2; Rare:85 | ||||
| chr9:128371184-128371404 | Rare:82 |