| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27370021-27370151 | Common:2; Rare:38 | ||||
| chr2:27370257-27370671 | Common:1; Rare:171 | ||||
| chr2:27380718-27380998 | Common:1; Rare:97; Clinvar:2 | ||||
| chr2:27409536-27409827 | Rare:114 | ||||
| chr2:27428435-27428724 | Common:1; Rare:113 | ||||
| chr2:27429000-27429247 | Common:1; Rare:77 | ||||
| chr2:27489686-27490031 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr2:27495196-27495382 | Rare:60 | ||||
| chr2:27582785-27583122 | Rare:113 | ||||
| chr2:27583466-27583975 | Common:1; Rare:145 | ||||
| chr2:27628955-27629096 | Common:1; Rare:74 | ||||
| chr2:27663620-27663966 | Common:1; Rare:135 | ||||
| chr2:27771591-27772035 | Common:1; Rare:139 | ||||
| chr2:27890563-27890792 | Rare:64 | ||||
| chr2:28392468-28392885 | Rare:137 |