| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:65373706-65373918 | Rare:72 | ||||
| chr7:65982140-65982328 | Common:3; Rare:66; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114748-66114919 | Common:1; Rare:79 | ||||
| chr7:66115177-66115353 | Common:1; Rare:41 | ||||
| chr7:66352302-66352554 | Common:3; Rare:56 | ||||
| chr7:66628670-66628990 | Common:2; Rare:116; Clinvar:5 | ||||
| chr7:66681966-66682229 | Common:6; Rare:111 | ||||
| chr7:66921072-66921469 | Common:1; Rare:112 | ||||
| chr7:66996569-66996893 | Common:2; Rare:71 | ||||
| chr7:70776872-70776939 | Rare:19 | ||||
| chr7:72828132-72828452 | Common:1; Rare:97 | ||||
| chr7:72924983-72925042 | Rare:12 | ||||
| chr7:73308776-73308885 | Rare:46 | ||||
| chr7:73521929-73522043 | Rare:42 | ||||
| chr7:73557109-73557361 | Common:1; Rare:89 |