| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27212257-27212366 | Common:1; Rare:55 | ||||
| chr2:27323043-27323143 | Rare:26; Clinvar (benign):1 | ||||
| chr2:27356750-27356794 | Rare:9 | ||||
| chr2:27370282-27370641 | Common:1; Rare:149 | ||||
| chr2:27582999-27583101 | Rare:39 | ||||
| chr2:27628980-27629058 | Common:1; Rare:39 | ||||
| chr2:27663369-27663467 | Rare:28 | ||||
| chr2:27663560-27663924 | Rare:133 | ||||
| chr2:27890364-27890818 | Common:1; Rare:121 | ||||
| chr2:28751738-28752134 | Common:1; Rare:162 | ||||
| chr2:28870262-28870463 | Rare:80 | ||||
| chr2:32039761-32039851 | Rare:27 | ||||
| chr2:32165690-32165901 | Common:1; Rare:84 | ||||
| chr2:32627945-32628143 | Rare:64 | ||||
| chr2:33134571-33134639 | Rare:9 |