| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75994534-75994772 | Common:4; Rare:127 | ||||
| chr7:76047943-76048180 | Common:1; Rare:81 | ||||
| chr7:76302820-76303073 | Rare:111; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr7:77696236-77696465 | Rare:91 | ||||
| chr7:77798387-77798916 | Common:1; Rare:131 | ||||
| chr7:79453560-79454117 | Common:3; Rare:137 | ||||
| chr7:80919009-80919287 | Common:3; Rare:90 | ||||
| chr7:87152276-87152474 | Common:1; Rare:69 | ||||
| chr7:87345473-87345701 | Common:4; Rare:73 | ||||
| chr7:87876349-87876646 | Common:1; Rare:127 | ||||
| chr7:90211633-90211886 | Common:3; Rare:77 | ||||
| chr7:90346557-90346738 | Common:4; Rare:78 | ||||
| chr7:91880668-91880801 | Common:1; Rare:36 | ||||
| chr7:92134400-92134604 | Rare:65 | ||||
| chr7:92134711-92134873 | Common:3; Rare:47 |