| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:141220375-141220453 | Rare:11 | ||||
| chr4:141220782-141221032 | Rare:83 | ||||
| chr4:141636282-141637135 | Common:4; Rare:193 | ||||
| chr4:142405389-142405570 | Common:1; Rare:27 | ||||
| chr4:143184665-143184985 | Common:8; Rare:124 | ||||
| chr4:143337125-143337163 | Rare:19 | ||||
| chr4:143381853-143381991 | Rare:21 | ||||
| chr4:143513349-143513538 | Common:2; Rare:68 | ||||
| chr4:145098141-145098361 | Rare:77 | ||||
| chr4:145180564-145180824 | Common:1; Rare:70 | ||||
| chr4:145482869-145483001 | Rare:21 | ||||
| chr4:145619355-145619416 | Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:147480759-147481005 | Rare:43 | ||||
| chr4:147617207-147617455 | Common:1; Rare:58 | ||||
| chr4:147683967-147684322 | Common:1; Rare:143 |