| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15469781-15469896 | Common:1; Rare:25 | ||||
| chr4:15655232-15655459 | Common:2; Rare:91 | ||||
| chr4:15659855-15660108 | Common:1; Rare:52 | ||||
| chr4:15681474-15681875 | Common:4; Rare:139 | ||||
| chr4:15703024-15703146 | Common:1; Rare:29 | ||||
| chr4:16898395-16898462 | Rare:18 | ||||
| chr4:17577316-17577567 | Rare:117 | ||||
| chr4:17614548-17614657 | Common:2; Rare:47 | ||||
| chr4:17810687-17811025 | Common:3; Rare:103 | ||||
| chr4:20700322-20700441 | Rare:44 | ||||
| chr4:23889974-23890278 | Common:1; Rare:52 | ||||
| chr4:24584381-24584611 | Rare:79 | ||||
| chr4:25159922-25160092 | Rare:41 | ||||
| chr4:25160332-25160753 | Common:3; Rare:126; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233815-25234084 | Rare:106 |