| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38125625-38125859 | Common:1; Rare:80 | ||||
| chr3:38138596-38138819 | Common:2; Rare:84; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:39051944-39052073 | Common:1; Rare:49 | ||||
| chr3:39107562-39107680 | Common:2; Rare:39 | ||||
| chr3:39153485-39153750 | Common:3; Rare:87 | ||||
| chr3:39406580-39406761 | Common:2; Rare:78 | ||||
| chr3:40309486-40309826 | Common:9; Rare:119 | ||||
| chr3:40524832-40524970 | Common:1; Rare:34 | ||||
| chr3:41962030-41962382 | Common:5; Rare:87 | ||||
| chr3:42581771-42581834 | Rare:16 | ||||
| chr3:42581889-42582137 | Common:3; Rare:78 | ||||
| chr3:42582251-42582359 | Rare:30 | ||||
| chr3:42600356-42600777 | Common:3; Rare:163 | ||||
| chr3:42804427-42804663 | Common:2; Rare:71 | ||||
| chr3:42906369-42906430 | Common:1; Rare:18 |