| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56995424-56995632 | Common:1; Rare:45 | ||||
| chrX:57121407-57121609 | Common:1; Rare:46 | ||||
| chrX:63351310-63351567 | Common:2; Rare:61 | ||||
| chrX:63755041-63755299 | Rare:58 | ||||
| chrX:63785130-63785288 | Rare:35; Clinvar (pathogenic):1 | ||||
| chrX:64205652-64205977 | Common:1; Rare:56 | ||||
| chrX:65034698-65034859 | Common:1; Rare:33 | ||||
| chrX:65534713-65535040 | Common:2; Rare:77 | ||||
| chrX:68433373-68433573 | Rare:27 | ||||
| chrX:68498958-68499059 | Rare:23 | ||||
| chrX:68828836-68829025 | Rare:38 | ||||
| chrX:70289858-70290121 | Rare:47 | ||||
| chrX:70454871-70455202 | Rare:36 | ||||
| chrX:70931094-70931249 | Common:17; Rare:27 | ||||
| chrX:71068302-71068613 | Common:2; Rare:80 |