| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42654129-42654164 | Rare:6 | ||||
| chr3:42773206-42773357 | Common:1; Rare:44 | ||||
| chr3:42804138-42804677 | Common:2; Rare:158 | ||||
| chr3:42843692-42844033 | Common:2; Rare:45 | ||||
| chr3:42906316-42906363 | Rare:15 | ||||
| chr3:42979209-42979355 | Rare:42 | ||||
| chr3:43286459-43286654 | Common:2; Rare:86 | ||||
| chr3:43621914-43622316 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690821-43690993 | Common:3; Rare:93; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691556-43691623 | Common:1; Rare:12 | ||||
| chr3:44338319-44338815 | Common:8; Rare:164 | ||||
| chr3:44477621-44477758 | Common:1; Rare:30 | ||||
| chr3:44555111-44555217 | Rare:22 | ||||
| chr3:44584947-44584992 | Rare:5 | ||||
| chr3:44624927-44625103 | Common:2; Rare:49 |