Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:33726047-33726397 | Rare:48 | ||||
chrX:47224495-47224732 | Common:1; Rare:35 | ||||
chrX:55908140-55908448 | Rare:50 | ||||
chrX:56564388-56564696 | Common:1; Rare:42; Clinvar (benign):1 | ||||
chrX:73845102-73845221 | Rare:28 | ||||
chrX:74221528-74221605 | Rare:10 | ||||
chrX:74292497-74292743 | Rare:43 | ||||
chrX:74420567-74420939 | Common:2; Rare:95 | ||||
chrX:107676946-107677184 | Common:1; Rare:28 | ||||
chrX:111511487-111511690 | Common:1; Rare:22 | ||||
chrX:129678304-129678537 | Rare:43 | ||||
chrX:134549642-134549848 | Common:2; Rare:44 | ||||
chrX:136030389-136030568 | Common:1; Rare:28 | ||||
chrX:153766477-153766574 | Rare:14 | ||||
chrX:153953369-153953558 | Common:2; Rare:45 |