Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:47144668-47144794 | Rare:23 | ||||
chrX:47145123-47145305 | Rare:30 | ||||
chrX:47483169-47483229 | Common:1; Rare:9 | ||||
chrX:48508878-48509036 | Rare:30 | ||||
chrX:48574246-48574558 | Common:2; Rare:93 | ||||
chrX:56563463-56563660 | Rare:45; Clinvar:1 | ||||
chrX:57121461-57121625 | Common:1; Rare:40 | ||||
chrX:68498965-68499058 | Rare:22 | ||||
chrX:70289895-70290038 | Rare:31 | ||||
chrX:74614588-74614893 | Common:1; Rare:70 | ||||
chrX:75274450-75274717 | Common:2; Rare:55 | ||||
chrX:75523018-75523211 | Common:1; Rare:39 | ||||
chrX:77895404-77895726 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:81201884-81202177 | Rare:49 | ||||
chrX:101407902-101408295 | Common:5; Rare:71; Clinvar (benign):9 |