| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185984288-185984344 | Rare:5 | ||||
| chr3:186021806-186022109 | Rare:60 | ||||
| chr3:186097862-186098337 | Rare:86 | ||||
| chr3:186099227-186099489 | Common:2; Rare:42 | ||||
| chr3:186104078-186104314 | Common:1; Rare:51 | ||||
| chr3:186107381-186107414 | Rare:3 | ||||
| chr3:186107732-186107884 | Rare:45 | ||||
| chr3:186183000-186183197 | Rare:36 | ||||
| chr3:186209856-186210180 | Common:2; Rare:64 | ||||
| chr3:186248148-186248349 | Rare:30 | ||||
| chr3:186248357-186248426 | Common:1; Rare:12 | ||||
| chr3:186613686-186613828 | Rare:18 | ||||
| chr3:186614008-186614191 | Rare:39 | ||||
| chr3:186614491-186614596 | Rare:16 | ||||
| chr3:186614722-186615149 | Common:4; Rare:78; Clinvar (benign):1 |