| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23667307-23667632 | Common:2; Rare:100 | ||||
| chrX:23743130-23743612 | Common:8; Rare:85 | ||||
| chrX:23782884-23783428 | Common:6; Rare:116 | ||||
| chrX:23884003-23884121 | Common:1; Rare:20 | ||||
| chrX:23907692-23907792 | Common:1; Rare:27 | ||||
| chrX:23907827-23908181 | Common:1; Rare:75 | ||||
| chrX:24054625-24055037 | Common:1; Rare:97 | ||||
| chrX:24149594-24149771 | Rare:29 | ||||
| chrX:24151267-24151415 | Common:1; Rare:15 | ||||
| chrX:24465039-24465343 | Common:4; Rare:88 | ||||
| chrX:24693797-24693962 | Common:1; Rare:31 | ||||
| chrX:30308207-30308737 | Rare:109; Clinvar (pathogenic):4 | ||||
| chrX:30309382-30309446 | Rare:13 | ||||
| chrX:30653140-30653521 | Common:2; Rare:103 | ||||
| chrX:33211550-33211651 | Rare:20 |