| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143513865-143514027 | Rare:74 | ||||
| chr4:145098148-145098361 | Rare:75 | ||||
| chr4:145619306-145619407 | Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147480883-147481101 | Common:1; Rare:46 | ||||
| chr4:147684105-147684289 | Common:1; Rare:72 | ||||
| chr4:148442375-148442712 | Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:150581620-150581976 | Common:1; Rare:70 | ||||
| chr4:151015709-151015853 | Rare:69 | ||||
| chr4:152536060-152536276 | Rare:82 | ||||
| chr4:152779711-152780183 | Common:2; Rare:118 | ||||
| chr4:153788728-153788787 | Common:2; Rare:26 | ||||
| chr4:158172360-158172674 | Rare:49 | ||||
| chr4:158172885-158173038 | Rare:20 | ||||
| chr4:158173041-158173187 | Rare:21 | ||||
| chr4:158210456-158210550 | Common:1; Rare:24 |