| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24285072-24285354 | Common:4; Rare:78; Clinvar (benign):1 | ||||
| chr7:24757383-24757494 | Common:3; Rare:35 | ||||
| chr7:25125212-25125643 | Rare:177; Clinvar:3 | ||||
| chr7:26200570-26201013 | Common:2; Rare:214 | ||||
| chr7:26201361-26201555 | Rare:74 | ||||
| chr7:26201583-26201839 | Common:2; Rare:126 | ||||
| chr7:27740102-27740199 | Common:3; Rare:27 | ||||
| chr7:28180546-28180896 | Common:4; Rare:96 | ||||
| chr7:29194719-29194990 | Common:2; Rare:75 | ||||
| chr7:29989722-29989898 | Rare:69 | ||||
| chr7:30026631-30026957 | Rare:75 | ||||
| chr7:30134780-30135183 | Common:5; Rare:133 | ||||
| chr7:30504758-30505079 | Common:2; Rare:106 | ||||
| chr7:30594722-30594909 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):4 | ||||
| chr7:30682472-30682643 | Rare:57 |