| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:137532424-137532619 | Common:1; Rare:33 | ||||
| chr4:139177180-139177437 | Rare:72 | ||||
| chr4:139301291-139301583 | Common:4; Rare:92 | ||||
| chr4:139302457-139302562 | Common:1; Rare:18 | ||||
| chr4:139453674-139453696 | Rare:9 | ||||
| chr4:139453699-139454204 | Common:4; Rare:136; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556100-139556567 | Rare:98 | ||||
| chr4:140373380-140373717 | Common:3; Rare:135 | ||||
| chr4:140524052-140524231 | Rare:56 | ||||
| chr4:141636792-141637113 | Rare:69 | ||||
| chr4:143184634-143184998 | Common:9; Rare:142 | ||||
| chr4:143336517-143336937 | Rare:94 | ||||
| chr4:143337051-143337211 | Rare:62 | ||||
| chr4:143337234-143337260 | Rare:8 | ||||
| chr4:145098115-145098343 | Rare:75 |