| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47145068-47145346 | Rare:41 | ||||
| chrX:47482578-47482670 | Common:5; Rare:20; Clinvar:2 | ||||
| chrX:47482928-47483010 | Rare:15 | ||||
| chrX:47483169-47483252 | Common:2; Rare:12 | ||||
| chrX:47561015-47561216 | Common:1; Rare:38 | ||||
| chrX:47582175-47582490 | Rare:54 | ||||
| chrX:47659107-47659271 | Rare:46 | ||||
| chrX:47836795-47836972 | Common:1; Rare:38 | ||||
| chrX:48476060-48476247 | Rare:36 | ||||
| chrX:48508848-48509027 | Common:1; Rare:37 | ||||
| chrX:48574875-48575190 | Common:3; Rare:82 | ||||
| chrX:48911616-48911722 | Rare:27; Clinvar (benign):4 | ||||
| chrX:48957880-48958038 | Rare:42 | ||||
| chrX:48958320-48958406 | Rare:25 | ||||
| chrX:49002189-49002318 | Rare:37 |