| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47145097-47145278 | Rare:29 | ||||
| chrX:47482579-47482653 | Common:5; Rare:17; Clinvar:2 | ||||
| chrX:49073995-49074180 | Rare:45 | ||||
| chrX:49079872-49079980 | Rare:21 | ||||
| chrX:53422645-53422906 | Common:1; Rare:63 | ||||
| chrX:53434349-53434469 | Common:1; Rare:29 | ||||
| chrX:54530033-54530246 | Common:2; Rare:31 | ||||
| chrX:55000241-55000381 | Rare:29 | ||||
| chrX:68498968-68499049 | Rare:20 | ||||
| chrX:70289875-70290130 | Rare:48 | ||||
| chrX:77895421-77895741 | Rare:87; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201904-81202189 | Rare:50 | ||||
| chrX:101407897-101408214 | Common:5; Rare:59; Clinvar (benign):9 | ||||
| chrX:103376427-103376597 | Common:1; Rare:27 | ||||
| chrX:104156978-104157063 | Rare:14 |