Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:41904003-41904391 | Common:2; Rare:124 | ||||
chr5:41925147-41925339 | Common:2; Rare:76 | ||||
chr5:43043207-43043296 | Common:1; Rare:18 | ||||
chr5:43064833-43065134 | Rare:71 | ||||
chr5:43067346-43067545 | Rare:32 | ||||
chr5:43121369-43121660 | Common:1; Rare:111 | ||||
chr5:43397114-43397232 | Rare:20 | ||||
chr5:43483837-43483913 | Common:1; Rare:31 | ||||
chr5:43515133-43515302 | Common:3; Rare:63 | ||||
chr5:43603068-43603266 | Rare:51 | ||||
chr5:44808727-44808976 | Common:2; Rare:84 | ||||
chr5:52989224-52989357 | Common:4; Rare:38; Clinvar (benign):1 | ||||
chr5:53109730-53109890 | Common:1; Rare:78; Clinvar:2 | ||||
chr5:54310513-54310711 | Rare:63 | ||||
chr5:55307620-55308016 | Common:4; Rare:134 |