| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:35642227-35642403 | Rare:31 | ||||
| chr3:35679457-35679714 | Rare:37 | ||||
| chr3:36993056-36993559 | Common:2; Rare:172; Clinvar:26; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:36993727-36993852 | Rare:47 | ||||
| chr3:37176104-37176397 | Common:1; Rare:80 | ||||
| chr3:37243166-37243348 | Common:1; Rare:48 | ||||
| chr3:38164998-38165272 | Common:1; Rare:64 | ||||
| chr3:38165462-38165868 | Common:1; Rare:141 | ||||
| chr3:38346730-38346780 | Rare:17 | ||||
| chr3:39051917-39052065 | Common:1; Rare:52 | ||||
| chr3:39107539-39107745 | Common:4; Rare:63 | ||||
| chr3:39383281-39383660 | Common:3; Rare:81; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39406555-39406763 | Common:6; Rare:88 | ||||
| chr3:40309446-40309919 | Common:9; Rare:159 | ||||
| chr3:40457194-40457402 | Common:3; Rare:101 |