| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:61783590-61784030 | Rare:78 | ||||
| chr3:61807890-61808340 | Common:3; Rare:107 | ||||
| chr3:61997554-61997954 | Common:5; Rare:118 | ||||
| chr3:62007470-62007910 | Common:6; Rare:147 | ||||
| chr3:62010936-62011380 | Common:10; Rare:275 | ||||
| chr3:62874000-62874320 | Common:1; Rare:80 | ||||
| chr3:63047150-63047440 | Common:1; Rare:67 | ||||
| chr3:63135682-63136677 | Common:33; Rare:635 | ||||
| chr3:63490030-63490490 | Common:3; Rare:84 | ||||
| chr3:63576770-63577310 | Common:6; Rare:105 | ||||
| chr3:63645024-63645298 | Common:4; Rare:70 | ||||
| chr3:63645568-63645899 | Common:1; Rare:89 | ||||
| chr3:63847709-63848110 | Common:3; Rare:75 | ||||
| chr3:63863027-63863251 | Common:1; Rare:51 | ||||
| chr3:63912750-63913210 | Common:1; Rare:226; Clinvar (benign):1 |