| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:154516229-154516582 | Common:3; Rare:66 | ||||
| chrX:154546804-154547017 | Rare:72 | ||||
| chrX:154547232-154547377 | Rare:27 | ||||
| chrX:154547543-154547663 | Common:1; Rare:31; Clinvar (benign):1 | ||||
| chrX:154762492-154762966 | Common:4; Rare:108; Clinvar:2 | ||||
| chrX:154799444-154799844 | Common:3; Rare:88 | ||||
| chrX:155026661-155026844 | Common:1; Rare:40 | ||||
| chrX:155026900-155027220 | Rare:85 | ||||
| chrX:155027374-155027513 | Rare:22 | ||||
| chrX:155071134-155071533 | Common:1; Rare:88 | ||||
| chrX:155216199-155216521 | Rare:56 | ||||
| chrX:155264250-155264387 | Rare:32; Clinvar:1 | ||||
| chrX:155767432-155767832 | Common:27; Rare:363 |