| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:145098134-145098348 | Rare:72 | ||||
| chr4:145179672-145179822 | Rare:56 | ||||
| chr4:145180003-145180148 | Rare:42 | ||||
| chr4:145180449-145180596 | Common:1; Rare:49 | ||||
| chr4:145619340-145619402 | Rare:21 | ||||
| chr4:146522327-146522455 | Common:2; Rare:51 | ||||
| chr4:147617231-147617511 | Common:1; Rare:63 | ||||
| chr4:147684096-147684256 | Common:1; Rare:62 | ||||
| chr4:148442272-148442749 | Rare:140; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:148444613-148445030 | Common:4; Rare:108 | ||||
| chr4:150581682-150582025 | Common:1; Rare:68 | ||||
| chr4:151015214-151015340 | Rare:37 | ||||
| chr4:151226376-151226537 | Rare:26 | ||||
| chr4:151325596-151325803 | Common:3; Rare:55 | ||||
| chr4:151408860-151409299 | Common:6; Rare:135 |