| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75724412-75724687 | Common:1; Rare:80 | ||||
| chr4:76148370-76148556 | Common:3; Rare:59 | ||||
| chr4:76949569-76949859 | Common:1; Rare:90 | ||||
| chr4:77862660-77862872 | Common:2; Rare:79 | ||||
| chr4:82891108-82891321 | Common:1; Rare:83 | ||||
| chr4:82900526-82900691 | Rare:49 | ||||
| chr4:83455814-83456087 | Common:2; Rare:109 | ||||
| chr4:89837098-89837250 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:98261148-98261489 | Common:1; Rare:111 | ||||
| chr4:98929093-98929365 | Common:3; Rare:70 | ||||
| chr4:99088705-99088870 | Common:6; Rare:70 | ||||
| chr4:99894373-99894612 | Common:2; Rare:84 | ||||
| chr4:102826779-102826968 | Rare:57 | ||||
| chr4:102827443-102827854 | Common:4; Rare:136 | ||||
| chr4:102827978-102828291 | Common:3; Rare:106 |