| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:28409642-28410374 | Common:5; Rare:294 | ||||
| chr7:28686280-28686840 | Common:3; Rare:127 | ||||
| chr7:29146390-29146623 | Common:2; Rare:78 | ||||
| chr7:29194240-29194610 | Rare:102 | ||||
| chr7:29479713-29480200 | Common:8; Rare:215 | ||||
| chr7:29564126-29565148 | Common:3; Rare:272 | ||||
| chr7:29989756-29989947 | Rare:77 | ||||
| chr7:30026578-30027016 | Common:1; Rare:101 | ||||
| chr7:30028185-30028460 | Common:1; Rare:97 | ||||
| chr7:30284252-30284387 | Common:1; Rare:47 | ||||
| chr7:30478028-30478498 | Common:3; Rare:135 | ||||
| chr7:30478430-30478600 | Common:3; Rare:74 | ||||
| chr7:30504795-30505147 | Common:3; Rare:102 | ||||
| chr7:30594665-30594950 | Common:6; Rare:118; Clinvar:6; Clinvar (benign):10 | ||||
| chr7:30595142-30595542 | Common:2; Rare:110; Clinvar (benign):1 |