| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:168890795-168891009 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:168924018-168924418 | Rare:97; Clinvar:4; Clinvar (benign):1 | ||||
| chr4:175914054-175914162 | Rare:26 | ||||
| chr4:184537513-184537703 | Common:3; Rare:53 | ||||
| chr4:184783865-184783990 | Rare:36 | ||||
| chr4:184802080-184802368 | Rare:53 | ||||
| chr4:184813282-184813347 | Rare:14 | ||||
| chr4:184813557-184813693 | Common:2; Rare:27 | ||||
| chr4:184814977-184815258 | Common:2; Rare:67 | ||||
| chr4:184851090-184851195 | Rare:14 | ||||
| chr4:184853544-184853774 | Common:3; Rare:48 | ||||
| chr4:185287359-185287739 | Common:4; Rare:74 | ||||
| chr4:185287760-185288074 | Common:3; Rare:75 | ||||
| chr4:185372921-185373315 | Common:2; Rare:116 | ||||
| chr4:185375611-185375903 | Common:1; Rare:62 |