| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27051219-27051266 | Common:1; Rare:41 | ||||
| chr2:27051465-27051721 | Rare:79 | ||||
| chr2:27071577-27071965 | Common:2; Rare:111 | ||||
| chr2:27072145-27072517 | Common:1; Rare:74 | ||||
| chr2:27086444-27086851 | Common:6; Rare:118; Clinvar (benign):3 | ||||
| chr2:27123785-27123856 | Common:2; Rare:16 | ||||
| chr2:27134537-27134903 | Common:1; Rare:141 | ||||
| chr2:27211327-27211452 | Rare:32 | ||||
| chr2:27211722-27212182 | Common:4; Rare:158 | ||||
| chr2:27212192-27212470 | Common:2; Rare:139 | ||||
| chr2:27212742-27212809 | Rare:10 | ||||
| chr2:27217254-27217592 | Rare:139 | ||||
| chr2:27322193-27322436 | Rare:47 | ||||
| chr2:27322949-27323395 | Common:4; Rare:135; Clinvar (benign):1 | ||||
| chr2:27356153-27356347 | Common:1; Rare:43 |