| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53093870-53094239 | Rare:67 | ||||
| chrX:53187836-53187850 | |||||
| chrX:53224006-53224136 | Rare:20 | ||||
| chrX:54443955-54444076 | Rare:16 | ||||
| chrX:56564385-56564700 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chrX:68829750-68829849 | Rare:29 | ||||
| chrX:70426942-70427166 | Rare:38 | ||||
| chrX:73844441-73844651 | Rare:58 | ||||
| chrX:73844662-73845090 | Rare:123 | ||||
| chrX:73845117-73845410 | Rare:65 | ||||
| chrX:73845678-73845807 | Rare:34 | ||||
| chrX:73849713-73849934 | Common:1; Rare:55 | ||||
| chrX:73850622-73850763 | Common:4; Rare:48 | ||||
| chrX:73851634-73852030 | Common:1; Rare:99 | ||||
| chrX:73944211-73944377 | Common:1; Rare:46 |