| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:185586033-185586373 | Common:1; Rare:78 | ||||
| chr3:186361949-186362025 | Rare:16 | ||||
| chr3:186567291-186567420 | Common:3; Rare:34 | ||||
| chr3:186783248-186783639 | Common:1; Rare:170 | ||||
| chr3:186806449-186806567 | Rare:39 | ||||
| chr3:187737688-187738140 | Common:3; Rare:67 | ||||
| chr3:188152701-188153221 | Common:2; Rare:89 | ||||
| chr3:188153227-188153261 | Rare:1 | ||||
| chr3:188153692-188154021 | Common:1; Rare:59 | ||||
| chr3:188154060-188154230 | Rare:57 | ||||
| chr3:188208087-188208244 | Common:1; Rare:24 | ||||
| chr3:188212313-188213009 | Common:2; Rare:107 | ||||
| chr3:189100003-189100153 | Common:2; Rare:25 | ||||
| chr3:190120345-190120610 | Common:1; Rare:109; Clinvar (pathogenic):1 | ||||
| chr3:190120828-190120952 | Rare:35 |