| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90153908-90154237 | Rare:51 | ||||
| chr7:90154359-90154525 | Rare:44 | ||||
| chr7:90211614-90211994 | Common:5; Rare:111 | ||||
| chr7:90245077-90245274 | Common:1; Rare:62 | ||||
| chr7:90346573-90346733 | Common:3; Rare:69 | ||||
| chr7:90595855-90596016 | Common:6; Rare:53 | ||||
| chr7:91880672-91880812 | Common:1; Rare:39 | ||||
| chr7:91940806-91940989 | Common:4; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92134409-92134603 | Rare:61 | ||||
| chr7:92245820-92245974 | Rare:37; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528403-92528807 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93232176-93232379 | Common:2; Rare:41 | ||||
| chr7:94656114-94656382 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95396359-95396466 | Common:2; Rare:44 | ||||
| chr7:95596196-95596199 |