| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:25160344-25160710 | Common:3; Rare:112; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234010 | Rare:66 | ||||
| chr4:25312624-25312861 | Common:1; Rare:86 | ||||
| chr4:25377002-25377343 | Common:3; Rare:104 | ||||
| chr4:25914028-25914328 | Common:2; Rare:129 | ||||
| chr4:26319672-26319867 | Rare:56 | ||||
| chr4:26320633-26320877 | Common:1; Rare:106 | ||||
| chr4:26320905-26321046 | Rare:51; Clinvar (benign):1 | ||||
| chr4:26583675-26584169 | Common:1; Rare:100 | ||||
| chr4:26860568-26860825 | Common:3; Rare:89 | ||||
| chr4:30719798-30720105 | Common:2; Rare:60 | ||||
| chr4:30720232-30720432 | Common:1; Rare:52 | ||||
| chr4:30721970-30722166 | Common:1; Rare:63 | ||||
| chr4:36281481-36281645 | Rare:28 | ||||
| chr4:37244075-37244207 | Common:2; Rare:29 |