| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:150323414-150323581 | Common:1; Rare:44 | ||||
| chr7:150323596-150323751 | Rare:55 | ||||
| chr7:150341567-150341929 | Common:2; Rare:55 | ||||
| chr7:150379070-150379327 | Common:1; Rare:90 | ||||
| chr7:150737135-150737429 | Common:5; Rare:50 | ||||
| chr7:150800279-150800986 | Common:10; Rare:172 | ||||
| chr7:150801331-150801723 | Common:6; Rare:121 | ||||
| chr7:150803092-150803455 | Common:5; Rare:68 | ||||
| chr7:151063105-151063164 | Rare:21 | ||||
| chr7:151069982-151070277 | Common:1; Rare:87 | ||||
| chr7:151080785-151080979 | Rare:62 | ||||
| chr7:151082992-151083163 | Rare:32 | ||||
| chr7:151232382-151232528 | Common:1; Rare:48 | ||||
| chr7:151471408-151471601 | Common:1; Rare:41 | ||||
| chr7:151877087-151877663 | Common:4; Rare:148; Clinvar:4; Clinvar (benign):1 |