Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:41060121-41060165 | Rare:17 | ||||
chr13:48413089-48413178 | Rare:12 | ||||
chr13:50005637-50005759 | Common:1; Rare:30 | ||||
chr13:52194392-52194542 | Rare:44 | ||||
chr13:52617393-52617541 | Common:1; Rare:36 | ||||
chr13:76885086-76885361 | Rare:98 | ||||
chr13:76885431-76885762 | Common:1; Rare:120 | ||||
chr13:77052308-77052548 | Common:3; Rare:40 | ||||
chr13:77113482-77113500 | Rare:3 | ||||
chr13:87671164-87671392 | Common:1; Rare:65 | ||||
chr13:93227416-93227612 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr13:102394502-102394654 | Common:1; Rare:55 | ||||
chr13:110174457-110174642 | Rare:70; Clinvar (benign):1 | ||||
chr13:110187300-110187575 | Rare:47 | ||||
chr13:110192802-110192841 | Rare:4 |