Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41448419-41448763 | Common:4; Rare:90 | ||||
chr22:41523934-41524016 | Rare:31; Clinvar (benign):1 | ||||
chr22:41530808-41531089 | Rare:75 | ||||
chr22:41951952-41952279 | Common:3; Rare:71 | ||||
chr22:42318196-42318332 | Rare:29 | ||||
chr22:42369248-42369491 | Common:3; Rare:59 | ||||
chr22:42588067-42588173 | Common:2; Rare:21 | ||||
chr22:42601124-42601239 | Common:1; Rare:31 | ||||
chr22:46069832-46070061 | Rare:47 | ||||
chr22:47487080-47487244 | Rare:51 | ||||
chr22:50300314-50300561 | Common:5; Rare:69 | ||||
chr22:50466178-50466417 | Rare:87 | ||||
chr22:50756755-50756950 | Common:7; Rare:99 | ||||
chr22:50798752-50798853 | Rare:46 | ||||
chr3:3850689-3850837 | Common:1; Rare:29 |