| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44194330-44194700 | Rare:127 | ||||
| chr15:44195224-44195578 | Common:8; Rare:275 | ||||
| chr15:44288325-44288960 | Common:97; Rare:640 | ||||
| chr15:44426850-44427314 | Common:2; Rare:273 | ||||
| chr15:44427420-44427746 | Common:3; Rare:185 | ||||
| chr15:44427838-44428033 | Rare:51 | ||||
| chr15:44536521-44536915 | Common:1; Rare:127 | ||||
| chr15:44536849-44537441 | Common:8; Rare:481 | ||||
| chr15:44662870-44663307 | Common:5; Rare:202 | ||||
| chr15:44663355-44663880 | Common:1; Rare:348; Clinvar:29; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr15:44711267-44711604 | Rare:240; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr15:44728742-44729321 | Common:3; Rare:245 | ||||
| chr15:45023020-45023274 | Common:9; Rare:184 | ||||
| chr15:45187923-45188121 | Common:5; Rare:140 | ||||
| chr15:45200390-45200705 | Common:4; Rare:215 |