| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:146381510-146381900 | Common:2; Rare:53 | ||||
| chr4:148394005-148394190 | Common:2; Rare:21 | ||||
| chr4:149951500-149951900 | Common:4; Rare:111 | ||||
| chr4:149955778-149956542 | Common:7; Rare:194 | ||||
| chr4:150173988-150174454 | Common:8; Rare:168 | ||||
| chr4:150579040-150579964 | Common:4; Rare:487 | ||||
| chr4:151014386-151014691 | Rare:88; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:151671601-151672077 | Common:6; Rare:185 | ||||
| chr4:152102528-152103632 | Common:6; Rare:202 | ||||
| chr4:152259030-152259330 | Common:1; Rare:53 | ||||
| chr4:152368062-152368477 | Rare:152 | ||||
| chr4:152646382-152647023 | Common:12; Rare:241 | ||||
| chr4:153083519-153083671 | Common:1; Rare:34 | ||||
| chr4:153154267-153154395 | Rare:25 | ||||
| chr4:153248863-153249013 | Common:1; Rare:24 |