Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27441976-27442509 | Common:2; Rare:188 | ||||
chr2:27489669-27489953 | Rare:71; Clinvar (benign):1 | ||||
chr2:27495189-27495338 | Rare:53 | ||||
chr2:27582865-27583143 | Rare:96 | ||||
chr2:27628955-27629168 | Common:1; Rare:106 | ||||
chr2:27663365-27663477 | Rare:29 | ||||
chr2:27663528-27663921 | Rare:139 | ||||
chr2:27664142-27664439 | Common:2; Rare:108 | ||||
chr2:27771652-27772005 | Common:1; Rare:109 | ||||
chr2:27890346-27890834 | Common:1; Rare:134 | ||||
chr2:28392474-28392819 | Rare:110 | ||||
chr2:28751525-28752179 | Common:4; Rare:252 | ||||
chr2:28861041-28861191 | Rare:44 | ||||
chr2:28870248-28870454 | Rare:86 | ||||
chr2:28894519-28894920 | Rare:177 |