| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:19116762-19116914 | Rare:36; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:19117410-19117545 | Common:2; Rare:60 | ||||
| chr7:20217350-20217577 | Common:1; Rare:51 | ||||
| chr7:20330767-20331061 | Common:2; Rare:81 | ||||
| chr7:20331739-20331912 | Common:1; Rare:67 | ||||
| chr7:23105682-23105871 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181923-23182117 | Rare:82 | ||||
| chr7:23299197-23299437 | Common:2; Rare:127 | ||||
| chr7:23470329-23470563 | Rare:72 | ||||
| chr7:23531928-23532083 | Common:2; Rare:65 | ||||
| chr7:25125251-25125443 | Rare:79; Clinvar:3 | ||||
| chr7:26200634-26201557 | Common:3; Rare:403 | ||||
| chr7:26201595-26201800 | Common:2; Rare:111 | ||||
| chr7:26864556-26864840 | Common:3; Rare:87 | ||||
| chr7:27095982-27096233 | Rare:71 |