| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:25664274-25664629 | Common:1; Rare:106 | ||||
| chr3:25664882-25665128 | Common:2; Rare:84 | ||||
| chr3:25783377-25783641 | Common:2; Rare:86; Clinvar (benign):3 | ||||
| chr3:25790000-25790144 | Common:4; Rare:58 | ||||
| chr3:27369366-27369592 | Rare:50 | ||||
| chr3:28241439-28241791 | Common:2; Rare:121 | ||||
| chr3:28348592-28348756 | Rare:37 | ||||
| chr3:28348784-28349196 | Common:4; Rare:130 | ||||
| chr3:29280305-29280624 | Common:6; Rare:50 | ||||
| chr3:29280826-29281695 | Common:16; Rare:180 | ||||
| chr3:31532070-31532168 | Common:2; Rare:26 | ||||
| chr3:31532304-31532608 | Common:3; Rare:96 | ||||
| chr3:31532821-31533205 | Common:2; Rare:156; Clinvar (benign):2 | ||||
| chr3:32106368-32106689 | Common:4; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:32502749-32502938 | Rare:57 |