| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:163494417-163494807 | Common:3; Rare:156 | ||||
| chr4:165112796-165112995 | Common:1; Rare:66 | ||||
| chr4:168480285-168480536 | Common:1; Rare:60 | ||||
| chr4:168831875-168832128 | Common:3; Rare:68 | ||||
| chr4:169010223-169010456 | Common:1; Rare:69 | ||||
| chr4:169612538-169612748 | Common:4; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
| chr4:169620370-169620763 | Common:2; Rare:133 | ||||
| chr4:169660029-169660431 | Common:2; Rare:73 | ||||
| chr4:173168200-173168365 | Common:1; Rare:38 | ||||
| chr4:173168612-173168893 | Common:3; Rare:90 | ||||
| chr4:173334316-173334613 | Rare:77 | ||||
| chr4:173369783-173369910 | Common:1; Rare:40 | ||||
| chr4:173370668-173371014 | Common:2; Rare:88 | ||||
| chr4:174283618-174284056 | Common:1; Rare:97 | ||||
| chr4:174521932-174522237 | Common:6; Rare:76; Clinvar (benign):1; Clinvar (pathogenic):1 |