| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55161097-55161269 | Rare:49 | ||||
| chrX:55452052-55452182 | Rare:23 | ||||
| chrX:56563363-56563658 | Common:1; Rare:59; Clinvar:1 | ||||
| chrX:56729468-56729567 | Common:1; Rare:12 | ||||
| chrX:56995446-56995625 | Common:1; Rare:41 | ||||
| chrX:57121422-57121643 | Common:1; Rare:52 | ||||
| chrX:63785120-63785310 | Rare:44; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:64205682-64206001 | Common:1; Rare:57 | ||||
| chrX:65034697-65034829 | Common:1; Rare:26 | ||||
| chrX:68433345-68433648 | Rare:51 | ||||
| chrX:68498965-68499056 | Rare:22 | ||||
| chrX:68828837-68829051 | Common:1; Rare:42 | ||||
| chrX:70289875-70290130 | Rare:48 | ||||
| chrX:70454894-70455215 | Rare:35 | ||||
| chrX:71068287-71068681 | Common:2; Rare:92 |