| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:92590031-92590114 | Rare:34 | ||||
| chr7:92833902-92834092 | Rare:46 | ||||
| chr7:92835446-92835684 | Common:1; Rare:56 | ||||
| chr7:92836405-92836529 | Rare:23 | ||||
| chr7:92836534-92836598 | Rare:16 | ||||
| chr7:93232173-93232395 | Common:2; Rare:45 | ||||
| chr7:93890714-93890947 | Common:3; Rare:56 | ||||
| chr7:93921925-93922129 | Common:4; Rare:50 | ||||
| chr7:94004227-94004506 | Rare:79 | ||||
| chr7:94509707-94510087 | Rare:127 | ||||
| chr7:94656043-94656440 | Common:2; Rare:91; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:94907489-94907693 | Common:1; Rare:45 | ||||
| chr7:94908378-94908559 | Rare:36 | ||||
| chr7:95434884-95435137 | Common:1; Rare:110; Clinvar (benign):1 | ||||
| chr7:96709792-96709923 | Rare:42 |