| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:62165275-62165413 | Common:1; Rare:38 | ||||
| chr15:62390434-62390576 | Rare:76 | ||||
| chr15:63042444-63042859 | Common:6; Rare:132; Clinvar:6; Clinvar (benign):2 | ||||
| chr15:63042884-63042938 | Rare:14; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr15:63062248-63062645 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:63121664-63121872 | Rare:58 | ||||
| chr15:63122406-63122701 | Common:4; Rare:92 | ||||
| chr15:63157403-63157597 | Common:3; Rare:86 | ||||
| chr15:63157701-63157851 | Common:1; Rare:40 | ||||
| chr15:63189316-63189633 | Common:2; Rare:106 | ||||
| chr15:63277308-63277630 | Common:4; Rare:65 | ||||
| chr15:63381837-63381928 | Common:1; Rare:18 | ||||
| chr15:63504384-63504744 | Common:2; Rare:124 | ||||
| chr15:63833879-63834054 | Common:1; Rare:68 | ||||
| chr15:64093770-64094094 | Common:1; Rare:90 |