| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:87006879-87006938 | Rare:22 | ||||
| chr4:87391156-87391287 | Rare:48 | ||||
| chr4:87422507-87422699 | Common:1; Rare:54 | ||||
| chr4:87975658-87975772 | Common:1; Rare:20 | ||||
| chr4:89111376-89111575 | Common:2; Rare:75 | ||||
| chr4:89837122-89837423 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:92304190-92304318 | Rare:37 | ||||
| chr4:94207843-94207952 | Rare:43 | ||||
| chr4:94451703-94451987 | Common:4; Rare:91 | ||||
| chr4:98143462-98143649 | Common:1; Rare:45 | ||||
| chr4:98261310-98261493 | Common:1; Rare:58 | ||||
| chr4:98929020-98929378 | Common:3; Rare:104 | ||||
| chr4:98995457-98995837 | Common:6; Rare:131 | ||||
| chr4:99088689-99088891 | Common:6; Rare:98 | ||||
| chr4:99563668-99563805 | Rare:40 |