Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20446860-20447081 | Common:3; Rare:85 | ||||
chr2:20651061-20651271 | Rare:66 | ||||
chr2:24076205-24076594 | Rare:106 | ||||
chr2:24123256-24123526 | Common:1; Rare:72 | ||||
chr2:24971908-24972145 | Common:1; Rare:76 | ||||
chr2:26033771-26034159 | Common:4; Rare:143 | ||||
chr2:26244601-26244943 | Common:2; Rare:123; Clinvar:5; Clinvar (benign):6 | ||||
chr2:26345838-26346152 | Common:1; Rare:90 | ||||
chr2:26764230-26764305 | Rare:25 | ||||
chr2:27032845-27033004 | Rare:63 | ||||
chr2:27212266-27212391 | Common:2; Rare:66 | ||||
chr2:27323058-27323149 | Rare:23 | ||||
chr2:27356754-27357071 | Rare:91 | ||||
chr2:27370310-27370641 | Common:1; Rare:131 | ||||
chr2:27582982-27583106 | Rare:45 |