| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:138242240-138242642 | Common:1; Rare:85 | ||||
| chr4:139301291-139301583 | Common:4; Rare:92 | ||||
| chr4:139302460-139302639 | Common:2; Rare:36 | ||||
| chr4:139453668-139454204 | Common:5; Rare:150; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:140373357-140373717 | Common:3; Rare:142 | ||||
| chr4:141220780-141220993 | Rare:74 | ||||
| chr4:141636560-141637005 | Common:1; Rare:102 | ||||
| chr4:142405394-142405543 | Rare:24 | ||||
| chr4:143513394-143513765 | Common:2; Rare:113 | ||||
| chr4:143513865-143514027 | Rare:74 | ||||
| chr4:145098137-145098374 | Rare:81 | ||||
| chr4:145619327-145619396 | Rare:25 | ||||
| chr4:147684091-147684265 | Common:1; Rare:67 | ||||
| chr4:151015272-151015377 | Rare:26 | ||||
| chr4:151015718-151015861 | Rare:69 |