| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54440271-54440459 | Rare:41 | ||||
| chrX:54530068-54530294 | Common:2; Rare:31 | ||||
| chrX:55452009-55452182 | Rare:30 | ||||
| chrX:56729452-56729530 | Common:1; Rare:10 | ||||
| chrX:57121461-57121696 | Common:1; Rare:54 | ||||
| chrX:65034698-65034823 | Common:1; Rare:26 | ||||
| chrX:65588225-65588401 | Common:1; Rare:31 | ||||
| chrX:68498977-68499056 | Rare:18 | ||||
| chrX:70289875-70290104 | Rare:43 | ||||
| chrX:71111557-71111696 | Rare:16; Clinvar:2 | ||||
| chrX:75156277-75156388 | Common:2; Rare:26 | ||||
| chrX:75523015-75523212 | Common:1; Rare:41 | ||||
| chrX:76172727-76173079 | Rare:56 | ||||
| chrX:77895417-77895741 | Rare:89; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103962-78104326 | Common:4; Rare:134 |