| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90346596-90346754 | Common:4; Rare:70 | ||||
| chr7:90405357-90405609 | Common:2; Rare:32 | ||||
| chr7:90595877-90596025 | Common:6; Rare:54 | ||||
| chr7:90596243-90596337 | Rare:27 | ||||
| chr7:91264212-91264460 | Common:1; Rare:66 | ||||
| chr7:91880635-91880812 | Common:1; Rare:51 | ||||
| chr7:91940659-91941138 | Common:5; Rare:149; Clinvar:5; Clinvar (benign):3 | ||||
| chr7:92134171-92134258 | Rare:27 | ||||
| chr7:92134369-92134612 | Rare:77 | ||||
| chr7:92134628-92134891 | Common:4; Rare:75 | ||||
| chr7:92245793-92246269 | Common:6; Rare:117; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528370-92528838 | Common:4; Rare:151; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92836914-92837033 | Common:2; Rare:23 | ||||
| chr7:93232139-93232394 | Common:2; Rare:53 | ||||
| chr7:93574716-93574824 | Rare:19 |