Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:130524263-130524372 | Common:1; Rare:22 | ||||
chrX:131830523-131830779 | Rare:34 | ||||
chrX:132025264-132025591 | Common:1; Rare:49 | ||||
chrX:133970133-133970231 | Rare:14 | ||||
chrX:133979686-133979829 | Rare:15 | ||||
chrX:134549235-134549351 | Rare:20 | ||||
chrX:134549635-134549855 | Common:2; Rare:49 | ||||
chrX:136909295-136909456 | Rare:45 | ||||
chrX:137567287-137567520 | Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chrX:148128918-148129003 | Common:1; Rare:14 | ||||
chrX:154369437-154369732 | Common:1; Rare:48 | ||||
chrX:155623373-155623504 | Rare:17 |