| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37243166-37243356 | Common:1; Rare:49 | ||||
| chr3:37993875-37994181 | Common:1; Rare:85 | ||||
| chr3:38165437-38165860 | Common:1; Rare:142 | ||||
| chr3:38346690-38346857 | Rare:55 | ||||
| chr3:39051859-39052073 | Common:1; Rare:68 | ||||
| chr3:39052421-39052534 | Rare:37 | ||||
| chr3:39107562-39107762 | Common:4; Rare:64 | ||||
| chr3:39383257-39383660 | Common:3; Rare:88; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:39406574-39406758 | Common:2; Rare:79 | ||||
| chr3:39406926-39407060 | Common:3; Rare:53 | ||||
| chr3:40309471-40309824 | Common:9; Rare:123 | ||||
| chr3:40457201-40457388 | Common:3; Rare:91 | ||||
| chr3:40477045-40477216 | Common:1; Rare:44 | ||||
| chr3:40505853-40506159 | Rare:74 | ||||
| chr3:40524815-40525013 | Common:1; Rare:58 |