| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48003951-48004198 | Common:2; Rare:72 | ||||
| chrX:48071070-48071265 | Rare:19 | ||||
| chrX:48071376-48071508 | Common:1; Rare:16 | ||||
| chrX:48475857-48476345 | Rare:82 | ||||
| chrX:48508845-48509052 | Common:1; Rare:41 | ||||
| chrX:48521525-48521889 | Common:1; Rare:60 | ||||
| chrX:48574118-48574528 | Common:3; Rare:96 | ||||
| chrX:48574788-48575019 | Rare:68 | ||||
| chrX:48676306-48676618 | Common:1; Rare:66 | ||||
| chrX:48696583-48696777 | Rare:43 | ||||
| chrX:48801596-48802142 | Common:2; Rare:98 | ||||
| chrX:48802404-48802717 | Common:1; Rare:57 | ||||
| chrX:48898148-48898259 | Common:1; Rare:20 | ||||
| chrX:48911632-48911722 | Rare:21; Clinvar (benign):3 | ||||
| chrX:48918988-48919210 | Rare:44 |