| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127937816-127937979 | Common:2; Rare:45; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:128275929-128276307 | Common:5; Rare:172 | ||||
| chr9:128322414-128322621 | Common:1; Rare:58 | ||||
| chr9:128322784-128322896 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128371242-128371375 | Rare:41 | ||||
| chr9:128455941-128456190 | Common:1; Rare:78 | ||||
| chr9:128552408-128552597 | Rare:73; Clinvar:1 | ||||
| chr9:128684429-128684617 | Rare:41 | ||||
| chr9:128724095-128724485 | Common:4; Rare:128 | ||||
| chr9:128921966-128922318 | Common:1; Rare:76 | ||||
| chr9:128947604-128947716 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129753065-129753177 | Rare:23 | ||||
| chr9:129835217-129835486 | Common:2; Rare:109 | ||||
| chr9:130053854-130053929 | Common:1; Rare:24 | ||||
| chr9:130579450-130579671 | Common:3; Rare:85 |