| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71068310-71068584 | Common:2; Rare:72 | ||||
| chrX:71365889-71366226 | Common:4; Rare:63 | ||||
| chrX:71532787-71533137 | Common:1; Rare:71 | ||||
| chrX:72181556-72181805 | Common:2; Rare:69 | ||||
| chrX:72238962-72239163 | Common:1; Rare:52 | ||||
| chrX:74614483-74614793 | Common:1; Rare:71 | ||||
| chrX:75156268-75156369 | Common:2; Rare:26 | ||||
| chrX:75274632-75274702 | Common:2; Rare:13 | ||||
| chrX:76172725-76173148 | Rare:77 | ||||
| chrX:77895417-77895750 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103931-78104393 | Common:4; Rare:165 | ||||
| chrX:80809765-80810167 | Common:1; Rare:51 | ||||
| chrX:81201911-81202180 | Rare:48 | ||||
| chrX:87517617-87517793 | Common:1; Rare:34 | ||||
| chrX:87517796-87518140 | Common:2; Rare:73 |