| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9732318-9732368 | Rare:18 | ||||
| chr3:9749693-9750020 | Common:1; Rare:107 | ||||
| chr3:9750110-9750385 | Common:1; Rare:97 | ||||
| chr3:9750985-9751047 | Rare:18 | ||||
| chr3:9769900-9770057 | Common:1; Rare:41 | ||||
| chr3:9792371-9792518 | Rare:45 | ||||
| chr3:9792617-9793178 | Common:4; Rare:206 | ||||
| chr3:9793545-9793679 | Rare:31 | ||||
| chr3:9809186-9809298 | Rare:23 | ||||
| chr3:9809699-9809786 | Common:1; Rare:22 | ||||
| chr3:9810060-9810297 | Common:1; Rare:88 | ||||
| chr3:9843436-9843479 | Common:1; Rare:20 | ||||
| chr3:9843923-9844224 | Common:4; Rare:126 | ||||
| chr3:9890442-9890756 | Common:4; Rare:131; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:9890799-9891055 | Rare:78 |