| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:68828837-68829030 | Rare:38 | ||||
| chrX:70289888-70290099 | Rare:38 | ||||
| chrX:71068310-71068671 | Common:2; Rare:86 | ||||
| chrX:71096016-71096180 | Rare:22 | ||||
| chrX:71254681-71254766 | Common:1; Rare:9 | ||||
| chrX:71365899-71366031 | Common:3; Rare:19 | ||||
| chrX:73563115-73563324 | Common:1; Rare:28 | ||||
| chrX:75156269-75156315 | Common:1; Rare:11 | ||||
| chrX:75273788-75274226 | Rare:57 | ||||
| chrX:75274474-75274692 | Common:2; Rare:43 | ||||
| chrX:75523013-75523212 | Common:1; Rare:41 | ||||
| chrX:75523231-75523315 | Rare:12 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77910588-77910780 | Common:1; Rare:24 | ||||
| chrX:79367287-79367479 | Common:1; Rare:35 |