| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:21751158-21751251 | Rare:30 | ||||
| chr3:23805812-23806066 | Common:1; Rare:51 | ||||
| chr3:23916807-23917196 | Rare:143 | ||||
| chr3:23917634-23917971 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr3:25428107-25428391 | Rare:64 | ||||
| chr3:25783377-25783621 | Common:2; Rare:83; Clinvar (benign):3 | ||||
| chr3:25790000-25790132 | Common:4; Rare:53 | ||||
| chr3:26622711-26622778 | Rare:17 | ||||
| chr3:27369319-27369515 | Rare:43 | ||||
| chr3:28348607-28348721 | Rare:26 | ||||
| chr3:28348772-28349191 | Common:4; Rare:133 | ||||
| chr3:29280825-29281391 | Common:15; Rare:111 | ||||
| chr3:32106376-32106720 | Common:4; Rare:94; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502741-32502938 | Rare:57 | ||||
| chr3:32570636-32570994 | Common:1; Rare:156 |