| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151099547-151099713 | Common:3; Rare:77 | ||||
| chr4:151408909-151409267 | Common:4; Rare:115 | ||||
| chr4:152536084-152536394 | Common:2; Rare:115 | ||||
| chr4:152679918-152680097 | Rare:51 | ||||
| chr4:152779715-152780013 | Common:1; Rare:83 | ||||
| chr4:153789081-153789226 | Rare:25 | ||||
| chr4:158173021-158173043 | Rare:7 | ||||
| chr4:158671868-158672365 | Common:5; Rare:116; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723214-158723455 | Common:2; Rare:104 | ||||
| chr4:159103806-159104087 | Common:4; Rare:93 | ||||
| chr4:163494637-163494739 | Common:1; Rare:36 | ||||
| chr4:165327411-165327734 | Common:2; Rare:93 | ||||
| chr4:168831981-168832139 | Common:3; Rare:47 | ||||
| chr4:168898353-168898537 | Common:1; Rare:50; Clinvar:2 | ||||
| chr4:169620366-169620702 | Common:2; Rare:116 |