| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:152298600-152298867 | Common:1; Rare:73 | ||||
| chr3:152298942-152299229 | Common:2; Rare:91 | ||||
| chr3:152834410-152835350 | Common:14; Rare:272 | ||||
| chr3:153161932-153162317 | Rare:271 | ||||
| chr3:154121158-154121530 | Common:10; Rare:352 | ||||
| chr3:154324270-154324875 | Common:1; Rare:306 | ||||
| chr3:155744284-155745071 | Common:1; Rare:179 | ||||
| chr3:155745036-155745238 | Rare:51 | ||||
| chr3:155806196-155806387 | Common:2; Rare:56 | ||||
| chr3:155853623-155853899 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr3:155854250-155854877 | Common:2; Rare:436; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:155870228-155870804 | Common:6; Rare:417 | ||||
| chr3:156456856-156457440 | Common:10; Rare:181 | ||||
| chr3:156555045-156555428 | Common:5; Rare:364 | ||||
| chr3:156674227-156674795 | Common:13; Rare:357 |