| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64794261-64794476 | Common:4; Rare:64 | ||||
| chr7:64903109-64903333 | Common:2; Rare:67 | ||||
| chr7:65006631-65006856 | Common:2; Rare:69 | ||||
| chr7:65872901-65873074 | Common:3; Rare:49 | ||||
| chr7:65982126-65982369 | Common:3; Rare:75; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66075579-66075944 | Rare:98; Clinvar (benign):1 | ||||
| chr7:66114693-66114968 | Common:2; Rare:105 | ||||
| chr7:66115194-66115357 | Rare:36 | ||||
| chr7:66682009-66682166 | Common:5; Rare:76 | ||||
| chr7:66921108-66921242 | Rare:43 | ||||
| chr7:66996566-66996872 | Common:2; Rare:67 | ||||
| chr7:71131222-71131918 | Common:8; Rare:219 | ||||
| chr7:71131961-71132188 | Common:1; Rare:67 | ||||
| chr7:72336722-72336797 | Rare:36 | ||||
| chr7:72337273-72337488 | Common:2; Rare:86 |