| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:28986173-28986411 | Common:1; Rare:50 | ||||
| chr7:29684901-29685032 | Common:1; Rare:51 | ||||
| chr7:32728580-32728825 | Common:8; Rare:77 | ||||
| chr7:32942468-32942715 | Common:2; Rare:70 | ||||
| chr7:38335581-38335904 | Common:2; Rare:75 | ||||
| chr7:38358380-38358480 | Common:1; Rare:49 | ||||
| chr7:39733498-39733669 | Rare:37 | ||||
| chr7:43619364-43619713 | Common:2; Rare:76 | ||||
| chr7:43987810-43987883 | Rare:25 | ||||
| chr7:44039499-44039541 | Common:1; Rare:12 | ||||
| chr7:44107846-44108084 | Common:3; Rare:85; Clinvar (pathogenic):1 | ||||
| chr7:44467580-44467910 | Common:3; Rare:74 | ||||
| chr7:44986551-44986748 | Common:3; Rare:91 | ||||
| chr7:45192586-45192729 | Common:1; Rare:22 | ||||
| chr7:45768763-45769154 | Common:4; Rare:109 |