| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:142405383-142405543 | Rare:25 | ||||
| chr4:143184652-143185159 | Common:8; Rare:191 | ||||
| chr4:143185884-143185922 | Rare:10 | ||||
| chr4:143337165-143337191 | Rare:12 | ||||
| chr4:143513348-143513547 | Common:2; Rare:70 | ||||
| chr4:144645917-144646178 | Common:1; Rare:71 | ||||
| chr4:144646484-144646692 | Rare:54 | ||||
| chr4:145098141-145098369 | Rare:80 | ||||
| chr4:145180491-145180833 | Common:1; Rare:99 | ||||
| chr4:145619250-145619417 | Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147617235-147617455 | Common:1; Rare:49 | ||||
| chr4:147683869-147683899 | Rare:16 | ||||
| chr4:147683995-147684404 | Common:2; Rare:144 | ||||
| chr4:148442324-148442749 | Rare:125; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:150581722-150581986 | Rare:55 |