| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27213000-27213195 | Rare:59 | ||||
| chr2:27217115-27217394 | Common:1; Rare:79 | ||||
| chr2:27263031-27263210 | Rare:45 | ||||
| chr2:27282329-27282506 | Rare:26 | ||||
| chr2:27323050-27323135 | Rare:19; Clinvar (benign):1 | ||||
| chr2:27356750-27356855 | Rare:27 | ||||
| chr2:27356968-27357150 | Common:1; Rare:65 | ||||
| chr2:27370302-27370753 | Common:2; Rare:182 | ||||
| chr2:27628954-27629073 | Common:1; Rare:57 | ||||
| chr2:27663369-27663477 | Rare:29 | ||||
| chr2:27663552-27663924 | Rare:135 | ||||
| chr2:27772226-27772358 | Rare:15 | ||||
| chr2:27890354-27890836 | Common:1; Rare:134 | ||||
| chr2:28751701-28752134 | Common:2; Rare:181 | ||||
| chr2:28870256-28870437 | Rare:71 |