| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:147617301-147617455 | Rare:34 | ||||
| chr4:147684096-147684345 | Common:1; Rare:104 | ||||
| chr4:147732023-147732331 | Rare:111 | ||||
| chr4:151015707-151015812 | Rare:41 | ||||
| chr4:151099327-151099713 | Common:3; Rare:122 | ||||
| chr4:152679935-152680156 | Rare:52 | ||||
| chr4:152779739-152780009 | Common:1; Rare:71 | ||||
| chr4:154550360-154550530 | Rare:52 | ||||
| chr4:156970958-156971188 | Rare:35 | ||||
| chr4:158671830-158672348 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723214-158723463 | Common:2; Rare:107 | ||||
| chr4:163166832-163166964 | Common:2; Rare:42 | ||||
| chr4:163494400-163494745 | Common:3; Rare:134 | ||||
| chr4:164956871-164957021 | Common:2; Rare:49 | ||||
| chr4:164977607-164977727 | Rare:32 |