| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671880-158672383 | Common:4; Rare:116; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723339-158723433 | Common:2; Rare:47 | ||||
| chr4:163166856-163166944 | Common:2; Rare:26 | ||||
| chr4:168921330-168921741 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169620267-169620707 | Common:2; Rare:148 | ||||
| chr4:170026340-170026627 | Common:4; Rare:118 | ||||
| chr4:173168708-173168838 | Common:2; Rare:51 | ||||
| chr4:173333644-173333878 | Common:1; Rare:64 | ||||
| chr4:173369787-173369945 | Common:1; Rare:54 | ||||
| chr4:173370676-173371016 | Common:2; Rare:88 | ||||
| chr4:173530137-173530353 | Rare:47 | ||||
| chr4:174283618-174283950 | Common:1; Rare:66 | ||||
| chr4:174522487-174522780 | Common:1; Rare:65; Clinvar:4 | ||||
| chr4:176319804-176320042 | Common:2; Rare:94 | ||||
| chr4:177442377-177442511 | Rare:81; Clinvar:2 |