| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145098138-145098417 | Rare:90 | ||||
| chr4:145179675-145179733 | Rare:18 | ||||
| chr4:145619267-145619396 | Rare:55 | ||||
| chr4:147617239-147617452 | Common:1; Rare:46 | ||||
| chr4:147684118-147684289 | Common:1; Rare:67 | ||||
| chr4:151015699-151015881 | Rare:83 | ||||
| chr4:152779687-152780222 | Common:2; Rare:140 | ||||
| chr4:154550304-154550530 | Common:2; Rare:75 | ||||
| chr4:154612585-154612976 | Common:1; Rare:81; Clinvar:3 | ||||
| chr4:158172649-158172730 | Rare:14 | ||||
| chr4:158671825-158672166 | Common:4; Rare:93; Clinvar:1 | ||||
| chr4:158672173-158672340 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:158723206-158723463 | Common:2; Rare:110 | ||||
| chr4:163166372-163166425 | Rare:27 | ||||
| chr4:163166829-163166972 | Common:2; Rare:46 |