| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26345791-26346226 | Common:1; Rare:134 | ||||
| chr2:26764188-26764357 | Common:2; Rare:65 | ||||
| chr2:27032848-27033088 | Rare:87 | ||||
| chr2:27051542-27051728 | Rare:57 | ||||
| chr2:27071525-27071888 | Common:1; Rare:110 | ||||
| chr2:27078255-27078838 | Common:3; Rare:134 | ||||
| chr2:27086532-27086797 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr2:27211747-27212103 | Common:3; Rare:122 | ||||
| chr2:27212225-27212484 | Common:2; Rare:127 | ||||
| chr2:27323029-27323149 | Rare:34; Clinvar (benign):1 | ||||
| chr2:27356750-27356863 | Rare:30 | ||||
| chr2:27356961-27357205 | Common:2; Rare:90 | ||||
| chr2:27370277-27370648 | Common:1; Rare:152 | ||||
| chr2:27373870-27374149 | Common:1; Rare:96 | ||||
| chr2:27380502-27380901 | Common:2; Rare:141; Clinvar:7 |