Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:154486585-154486783 | Rare:37 | ||||
chrX:154490614-154490843 | Common:2; Rare:54 | ||||
chrX:154516120-154516504 | Common:4; Rare:76 | ||||
chrX:154547553-154547644 | Common:1; Rare:23; Clinvar (benign):1 | ||||
chrX:155026546-155026827 | Common:1; Rare:56 | ||||
chrX:155026913-155027068 | Rare:44 |