| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27496715-27496943 | Rare:52 | ||||
| chr2:27507728-27508035 | Common:2; Rare:89 | ||||
| chr2:27582982-27583101 | Rare:44 | ||||
| chr2:27628977-27629077 | Common:1; Rare:51 | ||||
| chr2:27663364-27663513 | Rare:37 | ||||
| chr2:27663533-27663938 | Rare:149 | ||||
| chr2:27890312-27890842 | Common:2; Rare:152 | ||||
| chr2:28392633-28392858 | Rare:81 | ||||
| chr2:28751499-28752134 | Common:4; Rare:255 | ||||
| chr2:28870262-28870454 | Rare:75 | ||||
| chr2:31233997-31234155 | Rare:43 | ||||
| chr2:31414684-31414937 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chr2:32010993-32011050 | Rare:17 | ||||
| chr2:32039761-32039851 | Rare:27 | ||||
| chr2:32165745-32165899 | Common:1; Rare:58 |