| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47233310-47233515 | Rare:32 | ||||
| chrX:47482567-47482713 | Common:5; Rare:35; Clinvar:4 | ||||
| chrX:47482916-47483051 | Rare:27 | ||||
| chrX:47483169-47483237 | Common:1; Rare:9 | ||||
| chrX:47659066-47659235 | Rare:50 | ||||
| chrX:47836791-47836969 | Common:1; Rare:39 | ||||
| chrX:48003951-48004113 | Rare:42 | ||||
| chrX:48475840-48476247 | Rare:72 | ||||
| chrX:48508845-48509027 | Common:1; Rare:38 | ||||
| chrX:48521571-48522061 | Common:3; Rare:84; Clinvar (benign):1 | ||||
| chrX:48574404-48574556 | Rare:59 | ||||
| chrX:48574846-48574963 | Rare:34 | ||||
| chrX:48597225-48597556 | Common:1; Rare:52 | ||||
| chrX:48597663-48597849 | Common:1; Rare:19 | ||||
| chrX:48696584-48696778 | Rare:44 |