| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141220791-141220956 | Rare:52 | ||||
| chr4:143513435-143513810 | Common:1; Rare:123 | ||||
| chr4:145098141-145098350 | Rare:73 | ||||
| chr4:147617217-147617463 | Common:1; Rare:58 | ||||
| chr4:147684112-147684298 | Common:1; Rare:75 | ||||
| chr4:150581804-150581976 | Rare:37 | ||||
| chr4:151099412-151099713 | Common:3; Rare:111 | ||||
| chr4:151409025-151409188 | Common:3; Rare:45 | ||||
| chr4:152779577-152780021 | Common:3; Rare:114 | ||||
| chr4:153257222-153257399 | Common:1; Rare:34 | ||||
| chr4:158671830-158672305 | Common:5; Rare:121; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723319-158723439 | Common:2; Rare:58 | ||||
| chr4:163166832-163167009 | Common:2; Rare:67 | ||||
| chr4:163494561-163494745 | Common:2; Rare:63 | ||||
| chr4:165112857-165113015 | Common:1; Rare:42 |