| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:48483050-48483500 | Common:3; Rare:102 | ||||
| chr4:48779342-48779830 | Common:6; Rare:320 | ||||
| chr4:48780089-48780657 | Common:4; Rare:178 | ||||
| chr4:48830821-48831125 | Common:1; Rare:107 | ||||
| chr4:51842762-51843209 | Common:1; Rare:128 | ||||
| chr4:51843338-51843620 | Rare:166 | ||||
| chr4:51844740-51844970 | Common:1; Rare:61 | ||||
| chr4:52038218-52038341 | Rare:52; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr4:52038485-52038885 | Common:3; Rare:114 | ||||
| chr4:52051840-52052230 | Common:5; Rare:85 | ||||
| chr4:52659158-52659545 | Common:1; Rare:122 | ||||
| chr4:52862146-52862343 | Common:9; Rare:88 | ||||
| chr4:53365986-53366239 | Rare:62 | ||||
| chr4:53377516-53377729 | Common:1; Rare:71 | ||||
| chr4:54064522-54064912 | Common:5; Rare:126 |