| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:42804427-42804657 | Common:2; Rare:68 | ||||
| chr3:43690817-43690983 | Common:2; Rare:87; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338714-44338797 | Common:3; Rare:28 | ||||
| chr3:44477646-44477695 | Rare:11 | ||||
| chr3:44729556-44729667 | Common:1; Rare:42 | ||||
| chr3:44761590-44761804 | Common:3; Rare:77 | ||||
| chr3:44861767-44861925 | Common:2; Rare:71 | ||||
| chr3:44976120-44976273 | Common:2; Rare:64 | ||||
| chr3:45689180-45689464 | Common:1; Rare:96 | ||||
| chr3:46407027-46407268 | Rare:45 | ||||
| chr3:46693668-46693807 | Common:1; Rare:31 | ||||
| chr3:46979542-46979852 | Common:1; Rare:74; Clinvar:1 | ||||
| chr3:47380812-47381068 | Rare:77 | ||||
| chr3:47475816-47476058 | Common:3; Rare:103 | ||||
| chr3:48088784-48089059 | Rare:89 |