| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66921168-66921242 | Rare:30 | ||||
| chr7:66996557-66996868 | Common:2; Rare:71 | ||||
| chr7:72828128-72828478 | Common:1; Rare:100 | ||||
| chr7:73683412-73683624 | Common:3; Rare:86 | ||||
| chr7:73738768-73739123 | Common:2; Rare:117 | ||||
| chr7:73769559-73769847 | Common:1; Rare:90 | ||||
| chr7:74174027-74174405 | Common:1; Rare:172 | ||||
| chr7:74254383-74254528 | Rare:67 | ||||
| chr7:75914911-75915160 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994512-75994772 | Common:4; Rare:132 | ||||
| chr7:76047950-76048187 | Common:2; Rare:81 | ||||
| chr7:76302490-76302715 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:76303007-76303075 | Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:77122281-77122642 | Common:2; Rare:74 | ||||
| chr7:77696122-77696493 | Common:1; Rare:143 |