Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:135021496-135021528 | Rare:3 | ||||
chrX:141176372-141176456 | Rare:15 | ||||
chrX:153766431-153766607 | Rare:26 | ||||
chrX:154357253-154357522 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):7 | ||||
chrX:154448685-154448947 | Rare:53 |