| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:84959547-84959613 | Common:1; Rare:21 | ||||
| chr3:87227186-87227519 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:88058895-88059322 | Common:3; Rare:167 | ||||
| chr3:88149605-88149775 | Common:1; Rare:41 | ||||
| chr3:88149851-88150055 | Common:5; Rare:79 | ||||
| chr3:89107550-89107751 | Common:1; Rare:52 | ||||
| chr3:93979912-93980231 | Common:4; Rare:122; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062877-94062906 | Rare:10 | ||||
| chr3:94062910-94063091 | Rare:41 | ||||
| chr3:96814113-96814137 | Rare:4 | ||||
| chr3:96814400-96814662 | Rare:104 | ||||
| chr3:96814941-96815030 | Rare:21 | ||||
| chr3:97764491-97764875 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:97972380-97972514 | Common:3; Rare:54 | ||||
| chr3:98522851-98523138 | Common:1; Rare:84 |