| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183697682-183697909 | Common:2; Rare:104 | ||||
| chr3:184017864-184018081 | Common:1; Rare:66 | ||||
| chr3:184135229-184135490 | Common:2; Rare:88; Clinvar:6 | ||||
| chr3:184185858-184186207 | Common:5; Rare:129 | ||||
| chr3:184248906-184249021 | Rare:54; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:184298964-184299269 | Common:2; Rare:91 | ||||
| chr3:184314428-184314663 | Common:3; Rare:71 | ||||
| chr3:184335853-184335956 | Rare:34 | ||||
| chr3:184711926-184712244 | Common:2; Rare:108 | ||||
| chr3:185152901-185153060 | Common:4; Rare:55 | ||||
| chr3:185282868-185283027 | Common:1; Rare:41 | ||||
| chr3:185498900-185499155 | Rare:93 | ||||
| chr3:185552541-185552619 | Common:1; Rare:11 | ||||
| chr3:185824981-185825219 | Rare:66 | ||||
| chr3:185937966-185938183 | Common:1; Rare:91 |