| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:140756088-140756154 | Rare:14 | ||||
| chr4:140756328-140756420 | Rare:19 | ||||
| chr4:143184863-143184985 | Common:3; Rare:47 | ||||
| chr4:145098146-145098404 | Rare:86 | ||||
| chr4:145619273-145619406 | Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:145938390-145938526 | Rare:28 | ||||
| chr4:147617243-147617446 | Common:1; Rare:45 | ||||
| chr4:147684096-147684391 | Common:1; Rare:110 | ||||
| chr4:148442375-148442761 | Rare:119; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:151015220-151015379 | Rare:45 | ||||
| chr4:151015708-151015884 | Rare:80 | ||||
| chr4:151099312-151099627 | Common:2; Rare:85 | ||||
| chr4:151760968-151761188 | Rare:75 | ||||
| chr4:152679870-152680170 | Rare:98 | ||||
| chr4:152779608-152780016 | Common:2; Rare:101 |