| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47129553-47129589 | Common:1; Rare:4 | ||||
| chrX:47209726-47210123 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chrX:47212146-47212863 | Common:1; Rare:101; Clinvar:3; Clinvar (benign):1 | ||||
| chrX:47224685-47224849 | Rare:31 | ||||
| chrX:48902998-48903245 | Rare:29; Clinvar:1 | ||||
| chrX:49156270-49156389 | Rare:25 | ||||
| chrX:49879149-49879383 | Rare:35 | ||||
| chrX:53093835-53094232 | Rare:73 | ||||
| chrX:55489832-55489834 | |||||
| chrX:55489836-55489962 | Rare:18 | ||||
| chrX:55908050-55908283 | Rare:39 | ||||
| chrX:63427394-63427627 | Rare:48 | ||||
| chrX:65669147-65669245 | Rare:13 | ||||
| chrX:66018684-66018960 | Rare:51 | ||||
| chrX:73827184-73827361 | Common:1; Rare:43 |