| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:148442315-148442760 | Rare:233; Clinvar:8; Clinvar (benign):6 | ||||
| chr4:151015188-151015359 | Rare:83 | ||||
| chr4:151015696-151015908 | Rare:138 | ||||
| chr4:151099327-151099629 | Common:6; Rare:147 | ||||
| chr4:151325295-151325933 | Common:6; Rare:254 | ||||
| chr4:151408840-151409233 | Common:10; Rare:227 | ||||
| chr4:152536003-152536482 | Common:7; Rare:322 | ||||
| chr4:152779695-152780179 | Common:3; Rare:192 | ||||
| chr4:153204230-153204537 | Common:3; Rare:102 | ||||
| chr4:153344534-153344743 | Common:4; Rare:63 | ||||
| chr4:153466217-153466398 | Common:3; Rare:81 | ||||
| chr4:154550347-154550523 | Rare:105 | ||||
| chr4:154590625-154590975 | Common:5; Rare:127; Clinvar (benign):5 | ||||
| chr4:154612542-154612964 | Common:2; Rare:157; Clinvar:5 | ||||
| chr4:156971561-156971676 | Common:1; Rare:34 |