| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75523009-75523175 | Common:1; Rare:37 | ||||
| chrX:75523181-75523307 | Rare:21 | ||||
| chrX:77895369-77895750 | Rare:112; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chrX:77899268-77899549 | Rare:70; Clinvar (benign):1 | ||||
| chrX:78103875-78104343 | Common:4; Rare:170 | ||||
| chrX:80335258-80335418 | Common:2; Rare:32 | ||||
| chrX:80809838-80810155 | Rare:40 | ||||
| chrX:81121608-81121863 | Common:2; Rare:40 | ||||
| chrX:81201867-81202637 | Common:2; Rare:119 | ||||
| chrX:85243697-85243923 | Common:2; Rare:36 | ||||
| chrX:85243931-85244007 | Rare:11 | ||||
| chrX:86047483-86047645 | Common:1; Rare:37 | ||||
| chrX:87517637-87518248 | Common:4; Rare:123 | ||||
| chrX:93673548-93673762 | Common:1; Rare:34 | ||||
| chrX:93673911-93674259 | Rare:39 |