| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151057871-151058229 | Common:4; Rare:92 | ||||
| chr7:151059494-151059716 | Common:1; Rare:67 | ||||
| chr7:151080716-151080947 | Rare:74 | ||||
| chr7:151232396-151232537 | Rare:48 | ||||
| chr7:151408914-151409303 | Common:2; Rare:106 | ||||
| chr7:151409950-151410157 | Rare:57 | ||||
| chr7:151410389-151410525 | Common:1; Rare:19 | ||||
| chr7:151439901-151440054 | Common:1; Rare:34 | ||||
| chr7:151440082-151440241 | Common:1; Rare:35 | ||||
| chr7:151519892-151520025 | Rare:33 | ||||
| chr7:151877079-151877676 | Common:4; Rare:151; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:152025583-152025807 | Rare:89 | ||||
| chr7:152435669-152435731 | Common:1; Rare:16 | ||||
| chr7:152676160-152676316 | Common:1; Rare:71 | ||||
| chr7:152759642-152759829 | Common:4; Rare:75 |