| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92179119-92179190 | Common:1; Rare:12 | ||||
| chr7:92241086-92241281 | Rare:51; Clinvar (pathogenic):3 | ||||
| chr7:92245837-92246007 | Common:2; Rare:42; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:92246099-92246528 | Common:3; Rare:163 | ||||
| chr7:92447364-92447516 | Common:2; Rare:54 | ||||
| chr7:92477505-92477683 | Common:1; Rare:37 | ||||
| chr7:92528261-92528838 | Common:4; Rare:187; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590304-92590483 | Common:1; Rare:68 | ||||
| chr7:92833910-92834007 | Rare:28 | ||||
| chr7:92836227-92836498 | Rare:46 | ||||
| chr7:93148351-93148656 | Common:1; Rare:44 | ||||
| chr7:93232173-93232417 | Common:2; Rare:55 | ||||
| chr7:94004279-94004505 | Rare:59 | ||||
| chr7:94394537-94395050 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:94425748-94426050 | Rare:93; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 |