| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:224039114-224039180 | Rare:16 | ||||
| chr2:224039234-224039432 | Rare:80 | ||||
| chr2:226799808-226800189 | Common:1; Rare:109 | ||||
| chr2:226835895-226836156 | Common:1; Rare:105 | ||||
| chr2:227164457-227164646 | Rare:34; Clinvar:3 | ||||
| chr2:227325117-227325630 | Common:8; Rare:191 | ||||
| chr2:227717985-227718136 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:227813663-227813987 | Common:1; Rare:72 | ||||
| chr2:227815278-227815561 | Common:2; Rare:61 | ||||
| chr2:227871570-227871728 | Common:5; Rare:56 | ||||
| chr2:229586853-229587046 | Rare:27 | ||||
| chr2:229714507-229714679 | Common:4; Rare:49 | ||||
| chr2:229921881-229922522 | Common:4; Rare:221 | ||||
| chr2:229922873-229922997 | Rare:31 | ||||
| chr2:229923161-229923248 | Rare:20 |