Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chrX:41337332-41337466 | Rare:22 | ||||
chrX:45760116-45760319 | Common:1; Rare:26 | ||||
chrX:45770088-45770319 | Rare:20 | ||||
chrX:45771223-45771508 | Rare:31 | ||||
chrX:47577691-47577934 | Common:2; Rare:36 | ||||
chrX:53093850-53094222 | Rare:68 | ||||
chrX:53094271-53094421 | Rare:26 | ||||
chrX:65679419-65679717 | Rare:42 | ||||
chrX:66018853-66018960 | Rare:23 | ||||
chrX:66022840-66023098 | Rare:45 | ||||
chrX:66027463-66027658 | Common:3; Rare:39 | ||||
chrX:66032718-66032814 | Common:1; Rare:22 | ||||
chrX:67545524-67545696 | Rare:39; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chrX:72126385-72126494 | Rare:7 | ||||
chrX:73821975-73822143 | Common:1; Rare:32 |