| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:46759360-46759571 | Rare:27 | ||||
| chrX:46836696-46837088 | Rare:138; Clinvar:5; Clinvar (benign):2 | ||||
| chrX:46911944-46912329 | Rare:100 | ||||
| chrX:46912330-46912669 | Rare:154 | ||||
| chrX:47144474-47144845 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chrX:47145050-47145341 | Rare:76 | ||||
| chrX:47190637-47190950 | Rare:43 | ||||
| chrX:47193401-47194480 | Common:5; Rare:241; Clinvar:3 | ||||
| chrX:47217726-47218261 | Common:1; Rare:151 | ||||
| chrX:47218645-47218895 | Rare:160 | ||||
| chrX:47219047-47219447 | Common:4; Rare:80 | ||||
| chrX:47232914-47233040 | Rare:72 | ||||
| chrX:47233220-47233575 | Rare:87 | ||||
| chrX:47233644-47233828 | Common:1; Rare:24 | ||||
| chrX:47482523-47482731 | Common:10; Rare:90; Clinvar:8 |