| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27356750-27356855 | Rare:27 | ||||
| chr2:27370282-27370641 | Common:1; Rare:149 | ||||
| chr2:27489705-27490123 | Common:1; Rare:103 | ||||
| chr2:27582797-27583101 | Rare:103 | ||||
| chr2:27628977-27629058 | Common:1; Rare:41 | ||||
| chr2:27663585-27663913 | Rare:117 | ||||
| chr2:27890387-27890829 | Common:1; Rare:115 | ||||
| chr2:28751689-28752172 | Common:2; Rare:204 | ||||
| chr2:28870256-28870448 | Rare:79 | ||||
| chr2:32039738-32039851 | Rare:35 | ||||
| chr2:32165752-32165898 | Common:1; Rare:54 | ||||
| chr2:32628033-32628111 | Rare:23 | ||||
| chr2:33599210-33599469 | Common:1; Rare:97 | ||||
| chr2:37084276-37084544 | Common:3; Rare:96 | ||||
| chr2:37231559-37231703 | Common:4; Rare:79; Clinvar (benign):3 |