| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76047964-76048194 | Common:2; Rare:73 | ||||
| chr7:76302481-76302777 | Common:3; Rare:112; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr7:76302780-76303111 | Common:1; Rare:152; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr7:76303771-76304131 | Common:2; Rare:182; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):12 | ||||
| chr7:77199407-77199430 | Rare:10 | ||||
| chr7:77199503-77199762 | Common:2; Rare:66 | ||||
| chr7:77696236-77696500 | Rare:117 | ||||
| chr7:77696797-77696967 | Rare:73 | ||||
| chr7:77798460-77798957 | Common:1; Rare:128 | ||||
| chr7:79453555-79454117 | Common:3; Rare:139 | ||||
| chr7:80918939-80919348 | Common:3; Rare:134 | ||||
| chr7:87152165-87152718 | Common:3; Rare:162 | ||||
| chr7:87193146-87193254 | Rare:45 | ||||
| chr7:87345476-87345701 | Common:4; Rare:71 | ||||
| chr7:87876294-87876641 | Common:2; Rare:156 |