| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847503-37847642 | Rare:35 | ||||
| chrX:38220813-38221044 | Rare:53 | ||||
| chrX:38327450-38327682 | Rare:55 | ||||
| chrX:41333396-41333536 | Rare:27 | ||||
| chrX:44542813-44543090 | Common:1; Rare:56 | ||||
| chrX:46545393-46545524 | Rare:23 | ||||
| chrX:46837059-46837090 | Rare:9; Clinvar:1 | ||||
| chrX:47078380-47078428 | Rare:4 | ||||
| chrX:47144474-47144813 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chrX:47145090-47145302 | Rare:32 | ||||
| chrX:47233225-47233441 | Rare:38 | ||||
| chrX:47482558-47482665 | Common:5; Rare:24; Clinvar:2 | ||||
| chrX:47483151-47483299 | Common:3; Rare:19 | ||||
| chrX:47560875-47561221 | Common:1; Rare:58 | ||||
| chrX:48476089-48476256 | Rare:34 |