Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:28795640-28795851 | Rare:49 | ||||
chr22:28799600-28799616 | Rare:3 | ||||
chr22:28801534-28801610 | Common:1; Rare:12 | ||||
chr22:29273795-29274060 | Common:2; Rare:72 | ||||
chr22:29330432-29330645 | Common:1; Rare:71 | ||||
chr22:30922240-30922350 | Rare:46 | ||||
chr22:36288725-36289301 | Common:2; Rare:174; Clinvar:6; Clinvar (benign):10 | ||||
chr22:36302585-36302934 | Rare:98; Clinvar (benign):1 | ||||
chr22:39521525-39521813 | Common:1; Rare:138 | ||||
chr22:41413842-41414053 | Common:1; Rare:62 | ||||
chr22:41518289-41518567 | Common:3; Rare:57; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:42882200-42882535 | Common:2; Rare:72 | ||||
chr22:46065255-46065273 | Rare:7 | ||||
chr22:46069855-46070056 | Rare:43 | ||||
chr22:47154760-47155078 | Common:3; Rare:79 |