| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:154550347-154550517 | Rare:57 | ||||
| chr4:156971023-156971227 | Common:1; Rare:32 | ||||
| chr4:156971782-156971992 | Common:1; Rare:79 | ||||
| chr4:158172354-158172668 | Rare:49 | ||||
| chr4:158172984-158173090 | Rare:20 | ||||
| chr4:158671849-158672393 | Common:5; Rare:135; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723216-158723270 | Rare:19 | ||||
| chr4:158723319-158723446 | Common:2; Rare:60 | ||||
| chr4:164956891-164957023 | Common:2; Rare:41 | ||||
| chr4:165112789-165113113 | Common:1; Rare:106 | ||||
| chr4:165327418-165327734 | Common:2; Rare:92 | ||||
| chr4:165874809-165874967 | Common:1; Rare:48 | ||||
| chr4:168831968-168832175 | Common:3; Rare:66 | ||||
| chr4:169010239-169010456 | Common:1; Rare:60 | ||||
| chr4:169620391-169620702 | Common:2; Rare:107 |