| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:64205667-64205988 | Common:1; Rare:57 | ||||
| chrX:65034717-65034838 | Common:1; Rare:24 | ||||
| chrX:65534672-65535023 | Common:2; Rare:90 | ||||
| chrX:65667538-65667803 | Rare:46 | ||||
| chrX:66639009-66639416 | Rare:33 | ||||
| chrX:67543862-67544057 | Rare:31 | ||||
| chrX:68433455-68433614 | Rare:32 | ||||
| chrX:68433776-68433942 | Rare:19 | ||||
| chrX:68498952-68499099 | Rare:35 | ||||
| chrX:68647620-68647688 | Rare:19 | ||||
| chrX:68828832-68829030 | Rare:40 | ||||
| chrX:70289860-70290150 | Rare:51 | ||||
| chrX:70455023-70455211 | Rare:21 | ||||
| chrX:71068283-71068675 | Common:2; Rare:91 | ||||
| chrX:71118462-71118757 | Common:1; Rare:58; Clinvar (benign):2 |