| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147684124-147684271 | Common:1; Rare:58 | ||||
| chr4:148442412-148442738 | Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:151015192-151015457 | Rare:70 | ||||
| chr4:151015704-151015861 | Rare:74 | ||||
| chr4:151099313-151099628 | Common:3; Rare:85 | ||||
| chr4:152679963-152680097 | Rare:18 | ||||
| chr4:152779729-152780016 | Common:1; Rare:81 | ||||
| chr4:154550346-154550523 | Rare:58 | ||||
| chr4:155667239-155667451 | Rare:50 | ||||
| chr4:158671825-158672343 | Common:5; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:163166829-163167024 | Common:2; Rare:75 | ||||
| chr4:165327408-165327722 | Common:2; Rare:87 | ||||
| chr4:168318740-168318842 | Rare:20 | ||||
| chr4:169010247-169010443 | Common:1; Rare:58 | ||||
| chr4:169660034-169660272 | Common:1; Rare:44 |