| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75994528-75994791 | Common:4; Rare:139 | ||||
| chr7:76047950-76048170 | Common:1; Rare:73 | ||||
| chr7:76302844-76303054 | Rare:94; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:77696232-77696460 | Rare:89 | ||||
| chr7:79453652-79454109 | Common:3; Rare:110 | ||||
| chr7:80918986-80919287 | Common:3; Rare:96 | ||||
| chr7:87152152-87152468 | Common:2; Rare:89 | ||||
| chr7:87345443-87345744 | Common:6; Rare:92 | ||||
| chr7:87876329-87876634 | Common:2; Rare:132 | ||||
| chr7:91880677-91880751 | Common:1; Rare:20 | ||||
| chr7:91940796-91940964 | Common:3; Rare:49; Clinvar:2 | ||||
| chr7:92134375-92134570 | Rare:62 | ||||
| chr7:92134716-92134890 | Common:3; Rare:53 | ||||
| chr7:92245880-92246024 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):4 | ||||
| chr7:92246111-92246274 | Common:3; Rare:47 |