| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961566-123961781 | Rare:28 | ||||
| chrX:132023108-132023306 | Rare:46 | ||||
| chrX:141177072-141177314 | Common:1; Rare:31 | ||||
| chrX:149540420-149540725 | Common:1; Rare:36 | ||||
| chrX:149540805-149541059 | Common:4; Rare:48 | ||||
| chrX:149938440-149938620 | Common:1; Rare:46 | ||||
| chrX:150568451-150568653 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chrX:151397051-151397290 | Common:4; Rare:121 | ||||
| chrX:152698649-152698805 | Rare:1 | ||||
| chrX:152733680-152733827 | Common:1; Rare:46 | ||||
| chrX:152769666-152769832 | |||||
| chrX:152830706-152831075 | Common:2; Rare:68 | ||||
| chrX:153599079-153599363 | Common:13; Rare:57 | ||||
| chrX:153724023-153724151 | Common:1; Rare:26 | ||||
| chrX:153794056-153794190 | Common:1; Rare:20 |