| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145098156-145098404 | Rare:84 | ||||
| chr4:145619273-145619416 | Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147684073-147684286 | Common:1; Rare:77 | ||||
| chr4:148442384-148442733 | Rare:104; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:151099313-151099627 | Common:2; Rare:85 | ||||
| chr4:152679889-152680161 | Rare:84 | ||||
| chr4:152779729-152780016 | Common:1; Rare:81 | ||||
| chr4:154550317-154550530 | Common:1; Rare:71 | ||||
| chr4:158172353-158172757 | Rare:68 | ||||
| chr4:158671868-158672329 | Common:5; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723368-158723471 | Rare:42 | ||||
| chr4:165327383-165327702 | Common:3; Rare:95 | ||||
| chr4:168480465-168480632 | Rare:27 | ||||
| chr4:169010238-169010477 | Common:1; Rare:71 | ||||
| chr4:169612561-169612835 | Common:5; Rare:79; Clinvar:2; Clinvar (benign):2 |