| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:47836791-47836984 | Common:1; Rare:43 | ||||
| chrX:48476049-48476256 | Rare:40 | ||||
| chrX:48508861-48509039 | Rare:34 | ||||
| chrX:48574869-48574974 | Rare:32 | ||||
| chrX:48597666-48597816 | Rare:16 | ||||
| chrX:48696584-48696777 | Rare:43 | ||||
| chrX:48898167-48898265 | Common:1; Rare:16 | ||||
| chrX:48911622-48911706 | Rare:20; Clinvar (benign):4 | ||||
| chrX:48918960-48919265 | Rare:59 | ||||
| chrX:49002171-49002543 | Common:2; Rare:65 | ||||
| chrX:49079822-49079932 | Rare:15 | ||||
| chrX:49171787-49172003 | Common:3; Rare:27 | ||||
| chrX:49200170-49200339 | Rare:46; Clinvar:1 | ||||
| chrX:50204763-50204787 | Rare:3 |