Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:53405511-53405860 | Rare:41; Clinvar (benign):2 | ||||
chrX:56564383-56564654 | Common:1; Rare:36; Clinvar (benign):1 | ||||
chrX:73845137-73845223 | Rare:20 | ||||
chrX:73944207-73944361 | Common:1; Rare:39 | ||||
chrX:74207330-74207434 | Common:1; Rare:21 | ||||
chrX:74292497-74292743 | Rare:43 | ||||
chrX:74420564-74420917 | Common:2; Rare:93 | ||||
chrX:103536077-103536372 | Common:1; Rare:28 | ||||
chrX:103538774-103538991 | Common:1; Rare:14 | ||||
chrX:104126980-104127006 | Rare:6 | ||||
chrX:107674914-107675024 | Rare:19 | ||||
chrX:107676937-107677165 | Rare:28 | ||||
chrX:108437717-108437897 | Rare:20 | ||||
chrX:125204288-125204564 | Rare:32 | ||||
chrX:136030403-136030644 | Common:1; Rare:36 |