| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48957920-48958163 | Common:1; Rare:49 | ||||
| chrX:48958317-48958701 | Common:1; Rare:74 | ||||
| chrX:49002109-49002567 | Common:2; Rare:83 | ||||
| chrX:49073940-49074202 | Rare:61 | ||||
| chrX:49079837-49079946 | Rare:16 | ||||
| chrX:49101169-49101452 | Common:2; Rare:60 | ||||
| chrX:49200151-49200393 | Rare:75; Clinvar:1 | ||||
| chrX:49269090-49269416 | Common:1; Rare:54 | ||||
| chrX:49269537-49269840 | Rare:61 | ||||
| chrX:49879426-49879611 | Rare:35 | ||||
| chrX:49922404-49922673 | Rare:64 | ||||
| chrX:50067509-50067631 | Rare:19; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:50067750-50067953 | Common:1; Rare:33; Clinvar:1 | ||||
| chrX:50204729-50204789 | Rare:7 | ||||
| chrX:50470801-50471069 | Rare:37 |