| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:71068261-71068668 | Common:2; Rare:91 | ||||
| chrX:71111522-71111676 | Rare:17; Clinvar:2 | ||||
| chrX:71118462-71118757 | Common:1; Rare:58; Clinvar (benign):2 | ||||
| chrX:71254681-71254808 | Common:1; Rare:12 | ||||
| chrX:71365896-71366250 | Common:4; Rare:65 | ||||
| chrX:71532818-71533152 | Rare:70 | ||||
| chrX:74614398-74614910 | Common:1; Rare:116 | ||||
| chrX:75156273-75156369 | Common:2; Rare:26 | ||||
| chrX:75273986-75274232 | Rare:35 | ||||
| chrX:75274492-75274706 | Common:2; Rare:46 | ||||
| chrX:75523013-75523134 | Rare:28 | ||||
| chrX:75523239-75523326 | Rare:10 | ||||
| chrX:76172943-76173163 | Rare:53 | ||||
| chrX:77895310-77895741 | Rare:124; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chrX:78104047-78104356 | Common:4; Rare:117 |