| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:136767228-136767386 | Common:1; Rare:29 | ||||
| chrX:138711651-138711855 | Common:2; Rare:41 | ||||
| chrX:139933005-139933189 | Rare:37 | ||||
| chrX:141177074-141177310 | Common:1; Rare:31 | ||||
| chrX:149505218-149505424 | Rare:67 | ||||
| chrX:149540899-149541048 | Common:3; Rare:29 | ||||
| chrX:149938434-149938639 | Common:2; Rare:50 | ||||
| chrX:151396980-151397264 | Common:5; Rare:130 | ||||
| chrX:151974694-151974993 | Common:1; Rare:78 | ||||
| chrX:152830708-152831094 | Common:2; Rare:68 | ||||
| chrX:152941478-152941715 | Common:2; Rare:57 | ||||
| chrX:153599024-153599461 | Common:17; Rare:91 | ||||
| chrX:153724306-153724867 | Common:3; Rare:133 | ||||
| chrX:153780855-153781071 | Common:1; Rare:64 | ||||
| chrX:153794274-153794698 | Common:1; Rare:132; Clinvar (benign):2 |