| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:40193359-40193673 | Common:1; Rare:53 | ||||
| chr4:40196822-40197073 | Rare:47 | ||||
| chr4:41214458-41214742 | Common:5; Rare:68 | ||||
| chr4:41256756-41256963 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41990357-41990580 | Common:1; Rare:77 | ||||
| chr4:44678352-44678714 | Common:1; Rare:133 | ||||
| chr4:44726547-44726642 | Rare:38 | ||||
| chr4:47463598-47463734 | Common:1; Rare:62 | ||||
| chr4:47485198-47485340 | Common:1; Rare:53 | ||||
| chr4:47914543-47914802 | Common:1; Rare:75 | ||||
| chr4:48341233-48341475 | Common:1; Rare:103 | ||||
| chr4:48780245-48780636 | Common:3; Rare:117 | ||||
| chr4:48830821-48831149 | Common:1; Rare:113 | ||||
| chr4:48906704-48906871 | Rare:40 | ||||
| chr4:51842810-51843204 | Common:1; Rare:115 |