| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66921123-66921459 | Common:1; Rare:98 | ||||
| chr7:66995469-66995770 | Rare:80 | ||||
| chr7:66996554-66996932 | Common:2; Rare:91 | ||||
| chr7:69598966-69599206 | Rare:47 | ||||
| chr7:69599449-69599954 | Common:2; Rare:114; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr7:70694633-70694900 | Rare:76 | ||||
| chr7:71131482-71131721 | Common:5; Rare:82 | ||||
| chr7:72337259-72337456 | Common:2; Rare:70 | ||||
| chr7:72828138-72828458 | Common:1; Rare:93 | ||||
| chr7:72924983-72925130 | Common:1; Rare:51 | ||||
| chr7:73308765-73308912 | Rare:53 | ||||
| chr7:73557173-73557370 | Common:1; Rare:75 | ||||
| chr7:73557566-73557787 | Common:2; Rare:77 | ||||
| chr7:73578518-73578827 | Common:10; Rare:106 | ||||
| chr7:73683383-73683667 | Common:4; Rare:133 |