| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25878423-25878656 | Common:1; Rare:66 | ||||
| chr2:25982236-25982594 | Common:1; Rare:86 | ||||
| chr2:26033566-26033607 | Rare:7 | ||||
| chr2:26033752-26034734 | Common:8; Rare:303 | ||||
| chr2:26244573-26244977 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345758-26346272 | Common:2; Rare:161 | ||||
| chr2:26764207-26764389 | Common:2; Rare:64 | ||||
| chr2:26785717-26786123 | Rare:104 | ||||
| chr2:26970334-26970675 | Rare:87 | ||||
| chr2:27032844-27033153 | Rare:101 | ||||
| chr2:27086508-27086822 | Common:6; Rare:98; Clinvar (benign):3 | ||||
| chr2:27118901-27119137 | Rare:56 | ||||
| chr2:27123747-27123852 | Common:2; Rare:22 | ||||
| chr2:27211769-27212103 | Common:3; Rare:115 | ||||
| chr2:27212217-27212402 | Common:2; Rare:101 |