| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141636565-141636649 | Rare:18 | ||||
| chr4:141636742-141636991 | Common:1; Rare:56 | ||||
| chr4:143184672-143185096 | Common:8; Rare:157 | ||||
| chr4:143336585-143336912 | Rare:74 | ||||
| chr4:145098134-145098361 | Rare:77 | ||||
| chr4:145619346-145619403 | Rare:20; Clinvar (benign):1 | ||||
| chr4:147617201-147617455 | Common:1; Rare:60 | ||||
| chr4:147684118-147684265 | Common:1; Rare:56 | ||||
| chr4:148442327-148442712 | Rare:110; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:151099529-151099706 | Common:3; Rare:79 | ||||
| chr4:151143927-151144197 | Common:3; Rare:69 | ||||
| chr4:152536054-152536378 | Common:2; Rare:123 | ||||
| chr4:152679951-152680237 | Common:1; Rare:61 | ||||
| chr4:152779721-152780160 | Common:2; Rare:114 | ||||
| chr4:154550372-154550530 | Rare:47 |