| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26764166-26764385 | Common:2; Rare:82 | ||||
| chr2:26764421-26764572 | Rare:36 | ||||
| chr2:26764675-26764743 | Rare:11 | ||||
| chr2:26764774-26764820 | Rare:8 | ||||
| chr2:26785466-26785591 | Common:2; Rare:17 | ||||
| chr2:26785635-26786162 | Common:1; Rare:131 | ||||
| chr2:26786514-26786633 | Common:1; Rare:19 | ||||
| chr2:26970326-26970416 | Rare:18 | ||||
| chr2:26970497-26970711 | Rare:68 | ||||
| chr2:27032794-27033085 | Rare:99 | ||||
| chr2:27050249-27051216 | Common:11; Rare:377 | ||||
| chr2:27051496-27051724 | Rare:72 | ||||
| chr2:27071590-27071910 | Common:1; Rare:95 | ||||
| chr2:27086280-27086409 | Common:1; Rare:25 | ||||
| chr2:27086461-27086833 | Common:6; Rare:112; Clinvar (benign):3 |