| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168480417-168480547 | Common:1; Rare:24 | ||||
| chr4:168921359-168921741 | Common:2; Rare:83; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:169010196-169010478 | Common:1; Rare:89 | ||||
| chr4:169620382-169620725 | Common:2; Rare:117 | ||||
| chr4:169757851-169758063 | Rare:65 | ||||
| chr4:173333638-173333887 | Common:1; Rare:68 | ||||
| chr4:173334276-173334613 | Rare:92 | ||||
| chr4:173369792-173369953 | Common:1; Rare:55 | ||||
| chr4:173370682-173370963 | Common:2; Rare:71 | ||||
| chr4:173530159-173530523 | Common:3; Rare:71 | ||||
| chr4:174283612-174283973 | Common:1; Rare:74 | ||||
| chr4:174522289-174522666 | Rare:116; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:176319805-176320028 | Common:2; Rare:85 | ||||
| chr4:176792305-176792436 | Rare:39 | ||||
| chr4:177442376-177442549 | Rare:103; Clinvar:2 |