| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44573881-44574101 | Common:3; Rare:76 | ||||
| chr7:44581810-44581841 | Rare:16 | ||||
| chr7:44582147-44582537 | Common:1; Rare:152 | ||||
| chr7:44606433-44606641 | Common:1; Rare:70 | ||||
| chr7:44606808-44607074 | Common:2; Rare:80 | ||||
| chr7:44748343-44748591 | Common:2; Rare:61 | ||||
| chr7:44796375-44796792 | Common:3; Rare:161 | ||||
| chr7:44796990-44797160 | Rare:56 | ||||
| chr7:44847981-44848309 | Common:3; Rare:103 | ||||
| chr7:44999593-44999747 | Common:4; Rare:58 | ||||
| chr7:44999756-44999829 | Common:1; Rare:26 | ||||
| chr7:44999986-45000342 | Common:1; Rare:85; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:45111624-45111806 | Common:1; Rare:72 | ||||
| chr7:47582059-47582213 | Common:1; Rare:53 | ||||
| chr7:47582479-47582506 | Rare:5 |