| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27212196-27212486 | Common:4; Rare:246 | ||||
| chr2:27212950-27213249 | Rare:224 | ||||
| chr2:27217109-27217612 | Common:1; Rare:457 | ||||
| chr2:27263008-27263250 | Rare:152 | ||||
| chr2:27322934-27323238 | Common:4; Rare:237; Clinvar (benign):3 | ||||
| chr2:27356070-27356340 | Common:3; Rare:151 | ||||
| chr2:27356348-27356590 | Common:2; Rare:176 | ||||
| chr2:27356628-27357318 | Common:5; Rare:314 | ||||
| chr2:27369006-27369809 | Common:3; Rare:311; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:27370179-27370744 | Common:5; Rare:587 | ||||
| chr2:27409338-27409877 | Rare:392 | ||||
| chr2:27428182-27428359 | Common:3; Rare:48 | ||||
| chr2:27428911-27429263 | Common:4; Rare:246 | ||||
| chr2:27429268-27430049 | Common:6; Rare:196 | ||||
| chr2:27433620-27434120 | Common:1; Rare:112 |