| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27040132-27040357 | Common:1; Rare:60 | ||||
| chr2:27071387-27071744 | Common:2; Rare:110 | ||||
| chr2:27078519-27079231 | Common:4; Rare:207; Clinvar:1 | ||||
| chr2:27086484-27086801 | Common:4; Rare:93; Clinvar (benign):1 | ||||
| chr2:27134640-27134766 | Common:1; Rare:47 | ||||
| chr2:27211774-27212177 | Common:4; Rare:145 | ||||
| chr2:27212225-27212372 | Common:1; Rare:77 | ||||
| chr2:27217087-27217556 | Common:1; Rare:158 | ||||
| chr2:27323007-27323224 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr2:27356167-27356286 | Rare:28 | ||||
| chr2:27356721-27357199 | Common:2; Rare:144 | ||||
| chr2:27370200-27370792 | Common:2; Rare:230 | ||||
| chr2:27409464-27409756 | Rare:94 | ||||
| chr2:27429001-27429168 | Common:1; Rare:55 | ||||
| chr2:27433668-27433999 | Common:1; Rare:59 |