Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:85243832-85244151 | Common:2; Rare:62; Clinvar (benign):1 | ||||
chrX:96684682-96684906 | Rare:45 | ||||
chrX:100820291-100820434 | Common:1; Rare:32 | ||||
chrX:101348674-101348776 | Common:3; Rare:18 | ||||
chrX:101390818-101391046 | Rare:67 | ||||
chrX:101407806-101408292 | Common:5; Rare:88; Clinvar:2; Clinvar (benign):11 | ||||
chrX:101408373-101408476 | Rare:27 | ||||
chrX:101418249-101418306 | Rare:5 | ||||
chrX:102125557-102125776 | Common:2; Rare:44 | ||||
chrX:103214993-103215207 | Common:2; Rare:46 | ||||
chrX:103376441-103376607 | Common:1; Rare:24 | ||||
chrX:103585451-103585670 | Common:3; Rare:44 | ||||
chrX:103607759-103608020 | Common:1; Rare:44 | ||||
chrX:103686653-103687029 | Common:4; Rare:54 | ||||
chrX:103687068-103687283 | Rare:32 |