| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75914917-75915162 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76047806-76048196 | Common:3; Rare:122 | ||||
| chr7:76302873-76303073 | Rare:84; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:77696123-77696460 | Common:1; Rare:118 | ||||
| chr7:77798353-77798786 | Common:1; Rare:88 | ||||
| chr7:79453559-79453644 | Rare:24 | ||||
| chr7:79453659-79454121 | Common:3; Rare:111 | ||||
| chr7:87152324-87152628 | Common:2; Rare:87 | ||||
| chr7:87152648-87152733 | Rare:25 | ||||
| chr7:87345461-87345701 | Common:4; Rare:81 | ||||
| chr7:87876283-87876652 | Common:2; Rare:167 | ||||
| chr7:90211625-90211953 | Common:4; Rare:100 | ||||
| chr7:90346528-90346736 | Common:3; Rare:86 | ||||
| chr7:91880662-91880816 | Common:1; Rare:43 | ||||
| chr7:92134409-92134554 | Rare:41 |