| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27071604-27071882 | Common:1; Rare:87 | ||||
| chr2:27086594-27086797 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chr2:27211722-27212146 | Common:3; Rare:144 | ||||
| chr2:27212215-27212430 | Common:2; Rare:115 | ||||
| chr2:27217217-27217494 | Rare:105 | ||||
| chr2:27263044-27263181 | Rare:35 | ||||
| chr2:27323063-27323145 | Rare:21 | ||||
| chr2:27356750-27356863 | Rare:30 | ||||
| chr2:27356973-27357034 | Rare:21 | ||||
| chr2:27370283-27370641 | Common:1; Rare:148 | ||||
| chr2:27628993-27629127 | Common:1; Rare:75 | ||||
| chr2:27663369-27663488 | Rare:29 | ||||
| chr2:27663550-27663938 | Rare:145 | ||||
| chr2:27771655-27772009 | Common:1; Rare:109 | ||||
| chr2:27890387-27890822 | Common:1; Rare:113 |