| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139453774-139454148 | Common:3; Rare:92; Clinvar:9; Clinvar (benign):3 | ||||
| chr4:139556181-139556310 | Rare:31 | ||||
| chr4:140373380-140373701 | Common:2; Rare:129 | ||||
| chr4:141220801-141220971 | Rare:57 | ||||
| chr4:142405418-142405518 | Rare:16 | ||||
| chr4:145098141-145098361 | Rare:77 | ||||
| chr4:145619221-145619407 | Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:146945804-146946007 | Rare:53 | ||||
| chr4:147684133-147684242 | Rare:43 | ||||
| chr4:151015220-151015350 | Rare:39 | ||||
| chr4:151015718-151015818 | Rare:40 | ||||
| chr4:151099427-151099662 | Common:3; Rare:91 | ||||
| chr4:151408874-151409179 | Common:5; Rare:99 | ||||
| chr4:152679918-152680065 | Rare:46 | ||||
| chr4:152779653-152780009 | Common:2; Rare:93 |