Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:154486559-154486776 | Rare:34 | ||||
chrX:154490623-154490804 | Common:2; Rare:46 | ||||
chrX:154516120-154516537 | Common:4; Rare:83 | ||||
chrX:154547561-154547671 | Common:1; Rare:28; Clinvar (benign):1 | ||||
chrX:154762494-154762777 | Common:4; Rare:53 | ||||
chrX:155026680-155026881 | Common:1; Rare:48 | ||||
chrX:155026897-155027069 | Rare:48 | ||||
chrX:155071061-155071520 | Common:1; Rare:98 | ||||
chrY:19744705-19744797 | Rare:1 |