| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47233277-47233450 | Rare:28 | ||||
| chrX:47482586-47482665 | Common:5; Rare:18; Clinvar:2 | ||||
| chrX:47482928-47483030 | Rare:18 | ||||
| chrX:47483169-47483336 | Common:3; Rare:16 | ||||
| chrX:48476089-48476241 | Rare:29 | ||||
| chrX:48508855-48509032 | Rare:35 | ||||
| chrX:48696584-48696768 | Rare:41 | ||||
| chrX:48911632-48911722 | Rare:21; Clinvar (benign):3 | ||||
| chrX:49073995-49074193 | Rare:47 | ||||
| chrX:51893371-51893686 | Common:1; Rare:64 | ||||
| chrX:53082096-53082372 | Common:1; Rare:64 | ||||
| chrX:53422627-53422906 | Common:1; Rare:74 | ||||
| chrX:53536210-53536513 | Common:3; Rare:52; Clinvar (benign):1 | ||||
| chrX:54043926-54044048 | Rare:24 | ||||
| chrX:54440271-54440433 | Rare:28 |