| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27664246-27664570 | Common:1; Rare:100 | ||||
| chr2:27890344-27890834 | Common:1; Rare:135 | ||||
| chr2:28392626-28392917 | Rare:104 | ||||
| chr2:28751687-28752183 | Common:2; Rare:205 | ||||
| chr2:28870267-28870429 | Rare:60 | ||||
| chr2:31414647-31414937 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr2:32009916-32010145 | Common:1; Rare:72 | ||||
| chr2:32011000-32011189 | Rare:57 | ||||
| chr2:32039753-32039851 | Rare:29 | ||||
| chr2:32063362-32063692 | Common:1; Rare:117; Clinvar:1 | ||||
| chr2:32165745-32165898 | Common:1; Rare:57 | ||||
| chr2:32628031-32628125 | Rare:29 | ||||
| chr2:33476544-33476653 | Common:2; Rare:18 | ||||
| chr2:33599222-33599445 | Common:1; Rare:83 | ||||
| chr2:37084271-37084563 | Common:3; Rare:110 |