| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183253066-183253288 | Common:2; Rare:67 | ||||
| chr3:183635473-183635707 | Common:4; Rare:75 | ||||
| chr3:183884837-183884957 | Rare:51 | ||||
| chr3:184017864-184018053 | Rare:55 | ||||
| chr3:184135221-184135385 | Common:2; Rare:48; Clinvar:5 | ||||
| chr3:184185990-184186209 | Common:4; Rare:87 | ||||
| chr3:184248891-184249010 | Rare:62; Clinvar:5; Clinvar (benign):1 | ||||
| chr3:184298964-184299269 | Common:2; Rare:91 | ||||
| chr3:184711954-184712243 | Common:1; Rare:97 | ||||
| chr3:185282838-185283013 | Common:1; Rare:47 | ||||
| chr3:185498962-185499067 | Rare:46 | ||||
| chr3:185552541-185552619 | Common:1; Rare:11 | ||||
| chr3:185586000-185586358 | Common:1; Rare:81 | ||||
| chr3:186362203-186362303 | Rare:22 | ||||
| chr3:186567291-186567431 | Common:3; Rare:37 |