| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:337320-337952 | Common:13; Rare:399 | ||||
| chr4:474064-474363 | Common:3; Rare:105 | ||||
| chr4:499065-499378 | Common:9; Rare:318; Clinvar (benign):1 | ||||
| chr4:499656-500059 | Rare:86 | ||||
| chr4:663175-664150 | Common:3; Rare:375; Clinvar:1 | ||||
| chr4:664130-664430 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:673247-673906 | Common:4; Rare:259 | ||||
| chr4:674197-674688 | Common:9; Rare:558 | ||||
| chr4:687209-687488 | Rare:76 | ||||
| chr4:705519-705977 | Common:6; Rare:429 | ||||
| chr4:932046-932588 | Common:6; Rare:411 | ||||
| chr4:973476-973869 | Common:21; Rare:301 | ||||
| chr4:986829-987155 | Common:6; Rare:258; Clinvar:6; Clinvar (benign):3 | ||||
| chr4:987179-987531 | Common:1; Rare:211; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr4:992570-992990 | Common:3; Rare:237 |