| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:38220821-38220962 | Rare:24 | ||||
| chrX:41333865-41334183 | Common:3; Rare:81 | ||||
| chrX:46545393-46545524 | Rare:23 | ||||
| chrX:47144663-47144837 | Common:1; Rare:28 | ||||
| chrX:47145039-47145295 | Rare:36 | ||||
| chrX:47482548-47482654 | Common:5; Rare:24; Clinvar:2 | ||||
| chrX:47483169-47483277 | Common:3; Rare:14 | ||||
| chrX:47582194-47582474 | Rare:45 | ||||
| chrX:48476085-48476238 | Rare:28 | ||||
| chrX:48508880-48508992 | Rare:19 | ||||
| chrX:48574869-48574986 | Rare:34 | ||||
| chrX:48696583-48696761 | Rare:40 | ||||
| chrX:48898066-48898259 | Common:2; Rare:28 | ||||
| chrX:49079843-49079946 | Rare:16 | ||||
| chrX:53422613-53422918 | Common:2; Rare:82; Clinvar (benign):1 |