Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:48919019-48919229 | Rare:33 | ||||
chrX:49079863-49079988 | Rare:24 | ||||
chrX:53422605-53422826 | Common:1; Rare:66; Clinvar (benign):1 | ||||
chrX:53536210-53536513 | Common:3; Rare:52; Clinvar (benign):1 | ||||
chrX:54530033-54530294 | Common:2; Rare:41 | ||||
chrX:55161108-55161246 | Rare:41 | ||||
chrX:56563428-56563658 | Rare:47; Clinvar:1 | ||||
chrX:57121476-57121577 | Common:1; Rare:19 | ||||
chrX:65034711-65034823 | Common:1; Rare:25 | ||||
chrX:70289870-70290136 | Rare:50 | ||||
chrX:72239003-72239167 | Common:1; Rare:39 | ||||
chrX:81201867-81202169 | Rare:47 | ||||
chrX:96684704-96684906 | Rare:38 | ||||
chrX:101407891-101408282 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):10 | ||||
chrX:103686660-103686894 | Common:1; Rare:39 |