| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152536054-152536389 | Common:2; Rare:126 | ||||
| chr4:152779715-152780188 | Common:2; Rare:121 | ||||
| chr4:153789081-153789188 | Rare:18 | ||||
| chr4:154550372-154550525 | Rare:44 | ||||
| chr4:156971061-156971214 | Rare:22 | ||||
| chr4:158172369-158172734 | Rare:60 | ||||
| chr4:158172986-158173160 | Rare:29 | ||||
| chr4:158210299-158210589 | Common:3; Rare:71 | ||||
| chr4:158671866-158672359 | Common:5; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:159103819-159104158 | Common:4; Rare:121 | ||||
| chr4:163166832-163166931 | Common:2; Rare:34 | ||||
| chr4:165327400-165327734 | Common:2; Rare:97 | ||||
| chr4:165378946-165379093 | Common:2; Rare:39 | ||||
| chr4:168831881-168832106 | Common:2; Rare:58 | ||||
| chr4:168898281-168898537 | Common:1; Rare:62; Clinvar:2 |