| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54530064-54530305 | Common:2; Rare:35 | ||||
| chrX:55161108-55161274 | Rare:49 | ||||
| chrX:56729474-56729551 | Rare:9 | ||||
| chrX:57121453-57121591 | Common:1; Rare:32 | ||||
| chrX:64205690-64206011 | Common:1; Rare:57 | ||||
| chrX:65034698-65034863 | Common:1; Rare:34 | ||||
| chrX:68498965-68499058 | Rare:22 | ||||
| chrX:68828837-68829034 | Rare:40 | ||||
| chrX:73214788-73214986 | Common:1; Rare:25 | ||||
| chrX:74421371-74421501 | Rare:31; Clinvar (benign):1 | ||||
| chrX:75156273-75156369 | Common:2; Rare:26 | ||||
| chrX:75274645-75274691 | Common:1; Rare:8 | ||||
| chrX:75523003-75523170 | Rare:39 | ||||
| chrX:75523244-75523346 | Rare:13 | ||||
| chrX:77895398-77895732 | Rare:95; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 |