| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:208025492-208025506 | Rare:6 | ||||
| chr2:208025508-208025606 | Rare:21 | ||||
| chr2:208254232-208254482 | Rare:64 | ||||
| chr2:208254937-208255244 | Common:2; Rare:75 | ||||
| chr2:208266011-208266406 | Common:9; Rare:138; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423890-209424106 | Common:1; Rare:67 | ||||
| chr2:209771710-209772039 | Common:2; Rare:90 | ||||
| chr2:209960816-209960948 | Rare:27 | ||||
| chr2:210002495-210002765 | Common:4; Rare:105 | ||||
| chr2:210170727-210170878 | Rare:64 | ||||
| chr2:210171222-210171527 | Common:4; Rare:112 | ||||
| chr2:210225324-210225407 | Rare:13 | ||||
| chr2:210476659-210476867 | Rare:65 | ||||
| chr2:210477560-210477722 | Rare:48 | ||||
| chr2:210593264-210593425 | Common:1; Rare:32 |