| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66682009-66682207 | Common:6; Rare:94 | ||||
| chr7:66921130-66921252 | Rare:41 | ||||
| chr7:66995297-66995467 | Rare:71; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr7:66996557-66996888 | Common:2; Rare:77 | ||||
| chr7:72828138-72828458 | Common:1; Rare:93 | ||||
| chr7:73308786-73308890 | Rare:41 | ||||
| chr7:73557104-73557385 | Common:2; Rare:103 | ||||
| chr7:73557566-73557741 | Common:2; Rare:59 | ||||
| chr7:73683410-73683622 | Common:3; Rare:86 | ||||
| chr7:73738786-73739033 | Common:1; Rare:74 | ||||
| chr7:73842506-73842689 | Common:6; Rare:26 | ||||
| chr7:74174114-74174441 | Common:1; Rare:158 | ||||
| chr7:74254360-74254505 | Rare:66 | ||||
| chr7:74657459-74657730 | Common:2; Rare:80 | ||||
| chr7:75914911-75915186 | Common:3; Rare:97; Clinvar:3; Clinvar (benign):1 |