| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53422652-53422918 | Common:1; Rare:62 | ||||
| chrX:53686308-53686445 | Rare:22 | ||||
| chrX:54530070-54530314 | Common:2; Rare:34 | ||||
| chrX:68498961-68499072 | Rare:26 | ||||
| chrX:70289872-70290120 | Rare:46 | ||||
| chrX:73563371-73563488 | Rare:49 | ||||
| chrX:75274640-75274717 | Common:1; Rare:14 | ||||
| chrX:77895403-77895750 | Rare:96; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103866-78104305 | Common:4; Rare:156 | ||||
| chrX:81201887-81202159 | Rare:45 | ||||
| chrX:101407884-101408291 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:103356172-103356576 | Common:3; Rare:56 | ||||
| chrX:104156942-104157073 | Common:1; Rare:22 | ||||
| chrX:108091462-108091815 | Rare:95 | ||||
| chrX:111681031-111681221 | Rare:51; Clinvar (benign):4 |