| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153466426-153466581 | Common:3; Rare:44 | ||||
| chr4:153759509-153760126 | Common:7; Rare:184 | ||||
| chr4:153788110-153788893 | Common:9; Rare:420 | ||||
| chr4:153789038-153789235 | Rare:46 | ||||
| chr4:154491390-154491557 | Common:2; Rare:24 | ||||
| chr4:154491720-154492020 | Common:1; Rare:66 | ||||
| chr4:154550374-154550570 | Common:1; Rare:66 | ||||
| chr4:155376720-155377057 | Rare:85 | ||||
| chr4:155667029-155667782 | Common:4; Rare:264 | ||||
| chr4:155758800-155759060 | Common:1; Rare:61 | ||||
| chr4:156970560-156970980 | Common:3; Rare:101 | ||||
| chr4:156971065-156971285 | Common:2; Rare:36 | ||||
| chr4:156971610-156972070 | Common:4; Rare:151 | ||||
| chr4:157075860-157076210 | Rare:92; Clinvar (benign):1 | ||||
| chr4:158172920-158173240 | Rare:49 |