| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50350672-50350926 | Common:1; Rare:45 | ||||
| chr3:50350958-50351215 | Common:3; Rare:47 | ||||
| chr3:50365151-50365559 | Common:1; Rare:163; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:50567650-50567868 | Rare:68 | ||||
| chr3:50569465-50569584 | Common:1; Rare:28 | ||||
| chr3:50617111-50617229 | Common:3; Rare:17 | ||||
| chr3:50674889-50675024 | Rare:46 | ||||
| chr3:51384996-51385360 | Common:2; Rare:115 | ||||
| chr3:51391274-51391304 | Rare:10 | ||||
| chr3:51499948-51500076 | Rare:31 | ||||
| chr3:51500102-51500302 | Common:1; Rare:38 | ||||
| chr3:51941781-51942069 | Common:2; Rare:99 | ||||
| chr3:51968378-51968573 | Rare:36 | ||||
| chr3:51973542-51973715 | Rare:32 | ||||
| chr3:51974697-51974778 | Common:1; Rare:10 |