| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:37243194-37243483 | Common:1; Rare:70 | ||||
| chr3:37999044-37999342 | Common:5; Rare:92 | ||||
| chr3:38024464-38024667 | Common:1; Rare:79 | ||||
| chr3:38165474-38165813 | Common:1; Rare:116 | ||||
| chr3:38346708-38346897 | Rare:59 | ||||
| chr3:39051933-39052056 | Common:1; Rare:44 | ||||
| chr3:39107552-39107687 | Common:2; Rare:43 | ||||
| chr3:39383272-39383452 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383530-39383686 | Rare:34; Clinvar:2 | ||||
| chr3:39406574-39407015 | Common:4; Rare:171 | ||||
| chr3:40309491-40309890 | Common:9; Rare:133 | ||||
| chr3:40457194-40457397 | Common:3; Rare:99 | ||||
| chr3:40505934-40506132 | Rare:44 | ||||
| chr3:40524815-40524910 | Common:1; Rare:25 | ||||
| chr3:41199400-41199663 | Common:1; Rare:94 |