| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44123650-44123818 | Common:2; Rare:57 | ||||
| chr7:44490580-44490725 | Common:1; Rare:58 | ||||
| chr7:44573558-44574068 | Common:3; Rare:195 | ||||
| chr7:44582187-44582446 | Common:1; Rare:90 | ||||
| chr7:44606450-44606647 | Common:1; Rare:63 | ||||
| chr7:44796375-44796694 | Common:2; Rare:117 | ||||
| chr7:44798545-44798759 | Rare:43 | ||||
| chr7:44847969-44848471 | Common:4; Rare:149 | ||||
| chr7:44999576-44999848 | Common:5; Rare:102 | ||||
| chr7:44999925-45000358 | Common:1; Rare:105; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:45111642-45111799 | Common:1; Rare:63 | ||||
| chr7:45888187-45888506 | Rare:51 | ||||
| chr7:47280154-47280272 | Common:1; Rare:28 | ||||
| chr7:47581650-47581790 | Rare:29 | ||||
| chr7:47582050-47582232 | Common:1; Rare:61 |