| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141738066-141738437 | Common:4; Rare:122 | ||||
| chr7:143263457-143263528 | Rare:32 | ||||
| chr7:143380955-143381381 | Common:1; Rare:138 | ||||
| chr7:149028374-149028566 | Common:2; Rare:76 | ||||
| chr7:149147090-149147468 | Common:5; Rare:72 | ||||
| chr7:149261893-149262261 | Common:3; Rare:115 | ||||
| chr7:149460841-149460920 | Common:1; Rare:19 | ||||
| chr7:149873801-149874041 | Common:3; Rare:96 | ||||
| chr7:150800310-150800811 | Common:7; Rare:127 | ||||
| chr7:151249215-151249278 | Rare:16 | ||||
| chr7:155644384-155644471 | Rare:17 | ||||
| chr7:155644610-155644724 | Rare:49 | ||||
| chr7:157336768-157337013 | Common:1; Rare:107 | ||||
| chr8:232149-232397 | Common:3; Rare:97 | ||||
| chr8:6406527-6406673 | Common:3; Rare:79; Clinvar:2; Clinvar (benign):1 |