| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:123749559-123749615 | Rare:5 | ||||
| chr7:124929800-124929929 | Common:3; Rare:43 | ||||
| chr7:127392071-127392353 | Rare:111 | ||||
| chr7:127392666-127392967 | Common:1; Rare:81 | ||||
| chr7:127585566-127585707 | Common:2; Rare:48 | ||||
| chr7:127588259-127588530 | Rare:106 | ||||
| chr7:127651830-127652227 | Common:3; Rare:117 | ||||
| chr7:128241136-128241281 | Rare:43 | ||||
| chr7:128409942-128410044 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455736-128455903 | Common:2; Rare:93 | ||||
| chr7:128791241-128791499 | Common:1; Rare:63 | ||||
| chr7:129054867-129055239 | Common:2; Rare:70 | ||||
| chr7:129368016-129368361 | Rare:50 | ||||
| chr7:129611616-129611824 | Common:1; Rare:65 | ||||
| chr7:130070302-130070597 | Common:1; Rare:80 |