| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:156774524-156774717 | Common:5; Rare:33 | ||||
| chr4:158671849-158672353 | Common:5; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723202-158723474 | Common:2; Rare:116 | ||||
| chr4:163166832-163167081 | Common:2; Rare:92 | ||||
| chr4:165112827-165113041 | Common:1; Rare:65 | ||||
| chr4:168480471-168480567 | Rare:16 | ||||
| chr4:168630858-168631235 | Common:2; Rare:66 | ||||
| chr4:168631316-168631784 | Common:2; Rare:122 | ||||
| chr4:168649025-168649209 | Common:1; Rare:28 | ||||
| chr4:169010243-169010480 | Common:1; Rare:72 | ||||
| chr4:169612575-169612633 | Common:3; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620335-169620604 | Common:2; Rare:105 | ||||
| chr4:169620815-169620971 | Rare:29 | ||||
| chr4:169660036-169660288 | Common:1; Rare:46 | ||||
| chr4:169660515-169660576 | Rare:16 |