| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:80918852-80918874 | Rare:2 | ||||
| chr7:85186747-85186945 | Common:3; Rare:42 | ||||
| chr7:87152314-87152517 | Common:2; Rare:67 | ||||
| chr7:87345443-87345734 | Common:5; Rare:91 | ||||
| chr7:87876208-87876657 | Common:2; Rare:191 | ||||
| chr7:90245099-90245243 | Rare:51 | ||||
| chr7:90346573-90346736 | Common:3; Rare:69 | ||||
| chr7:91880668-91880801 | Common:1; Rare:36 | ||||
| chr7:91940771-91941048 | Common:4; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134376-92134594 | Rare:72 | ||||
| chr7:92134731-92134890 | Common:3; Rare:46 | ||||
| chr7:92245848-92245974 | Rare:35; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92246099-92246456 | Common:3; Rare:131 | ||||
| chr7:92528333-92528829 | Common:4; Rare:154; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92836285-92836489 | Rare:38 |