| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141220794-141221004 | Rare:74 | ||||
| chr4:142402763-142403274 | Common:2; Rare:105 | ||||
| chr4:142405117-142405609 | Common:3; Rare:125 | ||||
| chr4:142560208-142560268 | Rare:16 | ||||
| chr4:142846302-142846352 | Rare:9 | ||||
| chr4:143184639-143184914 | Common:9; Rare:110 | ||||
| chr4:143337095-143337195 | Rare:41 | ||||
| chr4:143513349-143513538 | Common:2; Rare:68 | ||||
| chr4:143513773-143513917 | Common:1; Rare:53 | ||||
| chr4:145098115-145098361 | Rare:81 | ||||
| chr4:145180538-145180857 | Common:1; Rare:90 | ||||
| chr4:145481641-145481703 | Rare:15 | ||||
| chr4:145619213-145619437 | Rare:89; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:145938389-145938589 | Common:1; Rare:40 | ||||
| chr4:145938786-145938969 | Rare:49 |