| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:131830618-131830773 | Rare:23 | ||||
| chrX:134549639-134550020 | Common:2; Rare:62 | ||||
| chrX:135033461-135033661 | Rare:25 | ||||
| chrX:136208145-136208636 | Rare:85; Clinvar:2; Clinvar (benign):4 | ||||
| chrX:149939981-149940071 | Rare:15 | ||||
| chrX:152905123-152905212 | Common:2; Rare:20 | ||||
| chrX:153703153-153703181 | Rare:4 | ||||
| chrX:153705372-153705579 | Rare:39 | ||||
| chrX:153706435-153706526 | Rare:13 | ||||
| chrX:153706705-153706884 | Common:4; Rare:25 | ||||
| chrX:153706973-153707271 | Rare:39 | ||||
| chrX:153925471-153925712 | Rare:45 | ||||
| chrX:154366092-154366369 | Common:3; Rare:83; Clinvar:8; Clinvar (benign):12 | ||||
| chrX:155054422-155054695 | Rare:48 | ||||
| chrX:155719042-155719232 | Common:1; Rare:42 |