| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949885-197950288 | Common:4; Rare:120; Clinvar (benign):2 | ||||
| chr3:197959969-197960259 | Common:1; Rare:100 | ||||
| chr4:124324-124535 | Common:6; Rare:59 | ||||
| chr4:337480-337883 | Common:3; Rare:117 | ||||
| chr4:499123-499351 | Common:3; Rare:97 | ||||
| chr4:663525-663727 | Common:1; Rare:65 | ||||
| chr4:673362-673554 | Rare:72 | ||||
| chr4:673829-673964 | Rare:53 | ||||
| chr4:674212-674596 | Common:4; Rare:179 | ||||
| chr4:681058-681232 | Rare:74 | ||||
| chr4:705593-705909 | Common:1; Rare:105 | ||||
| chr4:932207-932492 | Common:2; Rare:112 | ||||
| chr4:1113524-1113630 | Common:2; Rare:38 | ||||
| chr4:1289659-1289980 | Common:1; Rare:114 | ||||
| chr4:1720521-1720631 | Rare:30 |