Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:72248711-72248934 | Rare:43 | ||||
chr10:72297264-72297507 | Common:1; Rare:56 | ||||
chr10:73126205-73126331 | Common:1; Rare:28 | ||||
chr10:73232782-73233114 | Common:1; Rare:89 | ||||
chr10:73246758-73247004 | Rare:102 | ||||
chr10:73247166-73247362 | Rare:104 | ||||
chr10:73730456-73730617 | Common:1; Rare:39 | ||||
chr10:73805728-73805845 | Rare:23 | ||||
chr10:74095616-74095703 | Rare:21; Clinvar:4; Clinvar (benign):4 | ||||
chr10:74114586-74114863 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr10:74169105-74169182 | Common:1; Rare:14 | ||||
chr10:75230782-75230939 | Common:1; Rare:39 | ||||
chr10:76444073-76444382 | Rare:48 | ||||
chr10:77365948-77366263 | Common:3; Rare:64 | ||||
chr10:77552379-77552526 | Common:1; Rare:25 |