| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49171128-49171216 | Rare:18 | ||||
| chr3:49276929-49277213 | Common:2; Rare:102 | ||||
| chr3:49339914-49340439 | Common:3; Rare:162 | ||||
| chr3:49340455-49340660 | Common:1; Rare:36 | ||||
| chr3:49340665-49340916 | Common:1; Rare:53 | ||||
| chr3:49357965-49358103 | Common:1; Rare:71 | ||||
| chr3:49358253-49358649 | Common:3; Rare:173 | ||||
| chr3:49358720-49359055 | Common:2; Rare:78 | ||||
| chr3:49411854-49412517 | Common:2; Rare:241 | ||||
| chr3:49429225-49429505 | Common:1; Rare:72 | ||||
| chr3:49429686-49429869 | Common:1; Rare:40 | ||||
| chr3:49469713-49469853 | Rare:25 | ||||
| chr3:49469911-49470882 | Common:3; Rare:268; Clinvar (benign):2 | ||||
| chr3:49554324-49554517 | Rare:77 | ||||
| chr3:49673721-49674049 | Common:5; Rare:70 |