| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:21940613-21940869 | Common:2; Rare:63 | ||||
| chrX:23667361-23667591 | Common:2; Rare:71 | ||||
| chrX:23782918-23783423 | Common:5; Rare:111 | ||||
| chrX:23785292-23785857 | Common:1; Rare:93 | ||||
| chrX:23907699-23908007 | Common:1; Rare:65 | ||||
| chrX:24054607-24054710 | Common:2; Rare:20 | ||||
| chrX:24054891-24055037 | Rare:52 | ||||
| chrX:24149606-24149793 | Rare:34 | ||||
| chrX:24465099-24465347 | Common:4; Rare:71 | ||||
| chrX:30308216-30308772 | Rare:116; Clinvar (pathogenic):4 | ||||
| chrX:30309382-30309446 | Rare:13 | ||||
| chrX:30653140-30653450 | Common:2; Rare:82 | ||||
| chrX:31266899-31267043 | Common:1; Rare:45 | ||||
| chrX:37349179-37349404 | Common:2; Rare:34 | ||||
| chrX:37847500-37847677 | Common:1; Rare:43 |