| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27086601-27086790 | Rare:54 | ||||
| chr2:27211710-27212133 | Common:3; Rare:141 | ||||
| chr2:27212225-27212461 | Common:2; Rare:121 | ||||
| chr2:27217272-27217554 | Rare:122 | ||||
| chr2:27322932-27323161 | Rare:62; Clinvar (benign):1 | ||||
| chr2:27356139-27356286 | Rare:33 | ||||
| chr2:27356728-27356878 | Rare:37 | ||||
| chr2:27356961-27357170 | Common:2; Rare:72 | ||||
| chr2:27370257-27370674 | Common:1; Rare:171 | ||||
| chr2:27380537-27380940 | Common:2; Rare:155; Clinvar:7 | ||||
| chr2:27489705-27489931 | Rare:53 | ||||
| chr2:27582978-27583095 | Rare:42 | ||||
| chr2:27628957-27629101 | Common:1; Rare:79 | ||||
| chr2:27663336-27663929 | Rare:186 | ||||
| chr2:27771655-27771995 | Common:1; Rare:107 |