| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27086474-27086801 | Common:8; Rare:187; Clinvar (benign):2 | ||||
| chr2:27134496-27134776 | Common:1; Rare:211 | ||||
| chr2:27211742-27212200 | Common:8; Rare:265 | ||||
| chr2:27212225-27212484 | Common:4; Rare:250 | ||||
| chr2:27212977-27213265 | Rare:174 | ||||
| chr2:27217239-27217598 | Rare:145 | ||||
| chr2:27263010-27263280 | Common:1; Rare:101 | ||||
| chr2:27323022-27323166 | Common:2; Rare:79; Clinvar (benign):2 | ||||
| chr2:27356070-27356330 | Common:1; Rare:73 | ||||
| chr2:27356350-27356600 | Common:1; Rare:171 | ||||
| chr2:27356713-27356932 | Rare:89 | ||||
| chr2:27356968-27357227 | Common:4; Rare:177 | ||||
| chr2:27370257-27370679 | Common:3; Rare:325 | ||||
| chr2:27380698-27380894 | Common:2; Rare:113; Clinvar:4 | ||||
| chr2:27409434-27409811 | Rare:245 |