| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53083369-53083543 | Rare:25 | ||||
| chrX:53422613-53422908 | Common:2; Rare:81; Clinvar (benign):1 | ||||
| chrX:54530064-54530306 | Common:2; Rare:35 | ||||
| chrX:55452013-55452199 | Rare:33 | ||||
| chrX:56563508-56563660 | Rare:37; Clinvar:1 | ||||
| chrX:57121475-57121614 | Common:1; Rare:33 | ||||
| chrX:68498984-68499097 | Rare:27 | ||||
| chrX:71254102-71254350 | Common:1; Rare:44 | ||||
| chrX:71532847-71533153 | Rare:57 | ||||
| chrX:76172721-76173136 | Rare:72 | ||||
| chrX:77895398-77895753 | Rare:102; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77899194-77899523 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chrX:78103931-78104298 | Common:4; Rare:132 | ||||
| chrX:81201904-81202168 | Rare:45 | ||||
| chrX:81202331-81202512 | Common:2; Rare:28 |