Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:38738264-38738545 | Rare:56 | ||||
chr22:38981442-38981540 | Common:1; Rare:15 | ||||
chr22:39530196-39530387 | Rare:29 | ||||
chr22:39558064-39558094 | Rare:3 | ||||
chr22:40877541-40877754 | Rare:35 | ||||
chr22:41092835-41092855 | Rare:9 | ||||
chr22:41197439-41197633 | Common:2; Rare:49 | ||||
chr22:41325574-41325817 | Rare:62 | ||||
chr22:41327078-41327302 | Common:1; Rare:51 | ||||
chr22:41356404-41356678 | Common:1; Rare:80 | ||||
chr22:41413736-41414083 | Common:2; Rare:105 | ||||
chr22:41444411-41444414 | |||||
chr22:41522637-41523272 | Common:2; Rare:164; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr22:42369230-42369498 | Common:4; Rare:62 | ||||
chr22:42600936-42601229 | Common:1; Rare:59 |