| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173370682-173371012 | Common:2; Rare:85 | ||||
| chr4:173530205-173530478 | Common:2; Rare:59 | ||||
| chr4:174283316-174283363 | Rare:9 | ||||
| chr4:174283625-174283965 | Common:1; Rare:65 | ||||
| chr4:174522270-174522626 | Common:1; Rare:110; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522723-174522851 | Rare:21; Clinvar:1 | ||||
| chr4:176319624-176320028 | Common:4; Rare:117 | ||||
| chr4:177442311-177442519 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:182917319-182917584 | Common:4; Rare:84 | ||||
| chr4:183444342-183444765 | Common:2; Rare:184 | ||||
| chr4:183504522-183504842 | Common:3; Rare:104 | ||||
| chr4:183659112-183659401 | Common:1; Rare:98 | ||||
| chr4:184474497-184474826 | Rare:77 | ||||
| chr4:184649406-184649805 | Common:4; Rare:129 | ||||
| chr4:184734130-184734440 | Common:8; Rare:94 |