| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145098141-145098350 | Rare:73 | ||||
| chr4:145619081-145619416 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147617262-147617444 | Rare:40 | ||||
| chr4:147684127-147684309 | Rare:81 | ||||
| chr4:151099514-151099713 | Common:3; Rare:85 | ||||
| chr4:152679896-152680112 | Rare:68 | ||||
| chr4:152779730-152780005 | Common:1; Rare:76 | ||||
| chr4:156971095-156971183 | Rare:12 | ||||
| chr4:158172797-158172868 | Common:1; Rare:10 | ||||
| chr4:158671825-158672352 | Common:5; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723311-158723439 | Common:2; Rare:61 | ||||
| chr4:165327392-165327734 | Common:3; Rare:101 | ||||
| chr4:168480435-168480474 | Common:1; Rare:8 | ||||
| chr4:168480480-168480500 | Rare:4 | ||||
| chr4:169620253-169620598 | Common:2; Rare:121 |