Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:51893341-51893705 | Common:2; Rare:71 | ||||
chrX:53422605-53422918 | Common:2; Rare:87; Clinvar (benign):1 | ||||
chrX:53686586-53686828 | Common:6; Rare:55 | ||||
chrX:54043926-54044041 | Rare:23 | ||||
chrX:54530064-54530322 | Common:2; Rare:36 | ||||
chrX:55000194-55000390 | Rare:38 | ||||
chrX:55161101-55161269 | Rare:47 | ||||
chrX:55717546-55717812 | Rare:38 | ||||
chrX:56729471-56729559 | Common:1; Rare:11 | ||||
chrX:57121428-57121642 | Common:1; Rare:52 | ||||
chrX:68498965-68499059 | Rare:22 | ||||
chrX:68828837-68829076 | Common:1; Rare:46 | ||||
chrX:70289858-70290150 | Rare:51 | ||||
chrX:71254681-71254808 | Common:1; Rare:12 | ||||
chrX:71532894-71533146 | Rare:49 |