Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27323022-27323125 | Rare:30; Clinvar (benign):1 | ||||
chr2:27356750-27356855 | Rare:27 | ||||
chr2:27356957-27357170 | Common:2; Rare:73 | ||||
chr2:27370275-27370641 | Common:1; Rare:151 | ||||
chr2:27582797-27583122 | Rare:109 | ||||
chr2:27628981-27629099 | Common:1; Rare:65 | ||||
chr2:27663369-27663490 | Rare:30 | ||||
chr2:27663528-27663938 | Rare:150 | ||||
chr2:27890400-27890818 | Rare:107 | ||||
chr2:28392537-28392858 | Rare:109 | ||||
chr2:28751696-28752134 | Common:2; Rare:186 | ||||
chr2:28870262-28870475 | Rare:86 | ||||
chr2:31234009-31234158 | Rare:39 | ||||
chr2:32039738-32039860 | Rare:37 | ||||
chr2:32165732-32165898 | Common:1; Rare:63 |