| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139556166-139556514 | Rare:67 | ||||
| chr4:139665960-139666015 | Common:1; Rare:18 | ||||
| chr4:140373384-140373697 | Common:2; Rare:126 | ||||
| chr4:142405371-142405543 | Rare:30 | ||||
| chr4:143513630-143513742 | Rare:32 | ||||
| chr4:145098148-145098359 | Rare:74 | ||||
| chr4:145481511-145481703 | Rare:46 | ||||
| chr4:145482869-145483013 | Rare:25 | ||||
| chr4:145619296-145619396 | Rare:47 | ||||
| chr4:147617256-147617446 | Common:1; Rare:41 | ||||
| chr4:147684100-147684265 | Common:1; Rare:63 | ||||
| chr4:148442355-148442712 | Rare:103; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151015707-151015812 | Rare:41 | ||||
| chr4:151099511-151099713 | Common:3; Rare:85 | ||||
| chr4:151408861-151409209 | Common:5; Rare:114 |