| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:31981625-31981795 | Common:1; Rare:45 | ||||
| chr3:32106408-32106712 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32391742-32391955 | Common:3; Rare:58 | ||||
| chr3:32502747-32502956 | Rare:60 | ||||
| chr3:32570748-32570943 | Common:1; Rare:89 | ||||
| chr3:32685051-32685361 | Rare:96 | ||||
| chr3:33277331-33277499 | Common:1; Rare:47 | ||||
| chr3:33718061-33718308 | Rare:92 | ||||
| chr3:33798490-33798701 | Common:2; Rare:77 | ||||
| chr3:33798985-33799033 | Rare:15 | ||||
| chr3:36993064-36993550 | Common:2; Rare:162; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr3:37243166-37243392 | Common:1; Rare:57 | ||||
| chr3:38024472-38024668 | Common:1; Rare:75 | ||||
| chr3:39051944-39052060 | Common:1; Rare:43 | ||||
| chr3:39107203-39107451 | Common:4; Rare:52 |