| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27051394-27051794 | Rare:434 | ||||
| chr2:27071530-27072050 | Common:8; Rare:665 | ||||
| chr2:27086473-27086873 | Common:29; Rare:552; Clinvar (benign):14 | ||||
| chr2:27086976-27087376 | Common:1; Rare:108; Clinvar:4 | ||||
| chr2:27123609-27124009 | Common:6; Rare:147 | ||||
| chr2:27133780-27134409 | Common:4; Rare:209 | ||||
| chr2:27134482-27134882 | Common:4; Rare:469 | ||||
| chr2:27211119-27211519 | Rare:104 | ||||
| chr2:27211638-27212258 | Common:21; Rare:842 | ||||
| chr2:27212219-27212670 | Common:14; Rare:712 | ||||
| chr2:27212748-27213568 | Rare:539 | ||||
| chr2:27216980-27217580 | Common:2; Rare:688 | ||||
| chr2:27262955-27263355 | Common:2; Rare:290 | ||||
| chr2:27322141-27322582 | Rare:202; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
| chr2:27322810-27323362 | Common:9; Rare:448; Clinvar (benign):6 |