| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:124929793-124929915 | Common:3; Rare:41 | ||||
| chr7:124929921-124930013 | Rare:25 | ||||
| chr7:127585563-127585689 | Common:2; Rare:46 | ||||
| chr7:127588268-127588508 | Rare:99 | ||||
| chr7:127651957-127652227 | Common:1; Rare:83 | ||||
| chr7:128409899-128410072 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455663-128455919 | Common:3; Rare:129 | ||||
| chr7:128739159-128739431 | Common:1; Rare:71 | ||||
| chr7:128830467-128830506 | Rare:10 | ||||
| chr7:128830570-128830804 | Common:1; Rare:81; Clinvar:6; Clinvar (benign):5 | ||||
| chr7:128830806-128830989 | Rare:58; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:128841339-128841562 | Common:1; Rare:74; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr7:129054873-129055239 | Common:2; Rare:68 | ||||
| chr7:129611616-129611817 | Common:1; Rare:61 | ||||
| chr7:130070275-130070588 | Common:2; Rare:81 |