Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:17968784-17969119 | Common:3; Rare:120 | ||||
chr20:18467031-18467421 | Rare:84 | ||||
chr20:18507418-18507587 | Common:1; Rare:45 | ||||
chr20:20017214-20017399 | Rare:66 | ||||
chr20:21303281-21303385 | Rare:46 | ||||
chr20:24992698-24992818 | Common:3; Rare:58 | ||||
chr20:25195617-25195798 | Common:2; Rare:63 | ||||
chr20:25247952-25248104 | Common:1; Rare:56 | ||||
chr20:25407568-25407783 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr20:25623952-25624152 | Common:1; Rare:66 | ||||
chr20:25696800-25697066 | Common:3; Rare:77 | ||||
chr20:31547180-31547439 | Rare:63 | ||||
chr20:31723519-31723755 | Common:1; Rare:71 | ||||
chr20:31739109-31739375 | Common:1; Rare:70 | ||||
chr20:32207712-32207939 | Common:3; Rare:86 |