| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:128409954-128410088 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455702-128455966 | Common:5; Rare:235 | ||||
| chr7:128476643-128476913 | Common:2; Rare:175 | ||||
| chr7:128739144-128739439 | Common:4; Rare:154 | ||||
| chr7:128791240-128791480 | Common:2; Rare:119 | ||||
| chr7:129054300-129054660 | Common:2; Rare:131; Clinvar (benign):1 | ||||
| chr7:129054718-129055282 | Common:4; Rare:219; Clinvar (benign):4 | ||||
| chr7:129224340-129224670 | Rare:129 | ||||
| chr7:129224732-129225085 | Common:2; Rare:126 | ||||
| chr7:129434232-129434467 | Common:2; Rare:148 | ||||
| chr7:129611559-129611898 | Common:4; Rare:166 | ||||
| chr7:130051307-130051436 | Rare:58 | ||||
| chr7:130051356-130051471 | Common:1; Rare:37 | ||||
| chr7:130070090-130070603 | Common:4; Rare:183 | ||||
| chr7:130205250-130205574 | Common:4; Rare:284 |