| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:44019109-44019389 | Common:2; Rare:101 | ||||
| chr7:44038962-44039211 | Common:5; Rare:44 | ||||
| chr7:44107915-44108084 | Common:2; Rare:59; Clinvar (pathogenic):1 | ||||
| chr7:44467621-44467882 | Common:3; Rare:48 | ||||
| chr7:44986597-44986758 | Common:2; Rare:83 | ||||
| chr7:45187543-45187810 | Common:5; Rare:48 | ||||
| chr7:45192592-45192665 | Rare:10 | ||||
| chr7:45768887-45769158 | Common:4; Rare:82 | ||||
| chr7:47350220-47350471 | Rare:47 | ||||
| chr7:47475193-47475466 | Common:1; Rare:55 | ||||
| chr7:47476090-47476363 | Common:1; Rare:51 | ||||
| chr7:55039030-55039301 | Rare:42 | ||||
| chr7:55462631-55462724 | Common:2; Rare:17 | ||||
| chr7:65081199-65081403 | Common:3; Rare:71 | ||||
| chr7:65750908-65751094 | Common:2; Rare:79 |