| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147480662-147481010 | Rare:57 | ||||
| chr4:147617254-147617455 | Common:1; Rare:44 | ||||
| chr4:147684127-147684296 | Rare:70 | ||||
| chr4:148442319-148442712 | Rare:111; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015718-151015924 | Rare:87 | ||||
| chr4:151408874-151409193 | Common:5; Rare:102 | ||||
| chr4:152536079-152536261 | Rare:68 | ||||
| chr4:152779715-152780016 | Common:1; Rare:84 | ||||
| chr4:152936235-152936360 | Common:2; Rare:33 | ||||
| chr4:153204367-153204463 | Rare:20 | ||||
| chr4:158671868-158672382 | Common:5; Rare:121; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723327-158723463 | Common:2; Rare:61 | ||||
| chr4:165327411-165327748 | Common:2; Rare:99 | ||||
| chr4:168480468-168480515 | Rare:11 | ||||
| chr4:169620415-169620673 | Common:2; Rare:93 |