| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:25964546-25964848 | Common:1; Rare:46 | ||||
| chr7:26188732-26188811 | Common:1; Rare:37 | ||||
| chr7:26189556-26189744 | Rare:70 | ||||
| chr7:26193249-26193673 | Rare:148; Clinvar (benign):2 | ||||
| chr7:26863446-26863767 | Common:2; Rare:53 | ||||
| chr7:27118172-27118203 | Rare:9 | ||||
| chr7:27799918-27800022 | Rare:21 | ||||
| chr7:27834376-27834559 | Common:1; Rare:35 | ||||
| chr7:28955683-28955997 | Common:1; Rare:115 | ||||
| chr7:30284856-30285018 | Rare:54 | ||||
| chr7:30286079-30286425 | Common:1; Rare:75 | ||||
| chr7:30561537-30561765 | Common:4; Rare:40 | ||||
| chr7:32527354-32527457 | Rare:23 | ||||
| chr7:32569870-32570146 | Common:1; Rare:71 | ||||
| chr7:32728029-32728146 | Common:1; Rare:42 |