| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13652972-13653203 | Rare:53 | ||||
| chrX:13734529-13734866 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chrX:14029801-14029963 | Common:1; Rare:50 | ||||
| chrX:14873016-14873470 | Common:2; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:16712598-16712720 | Common:1; Rare:19 | ||||
| chrX:16786132-16786503 | Common:2; Rare:75 | ||||
| chrX:16870215-16870762 | Common:3; Rare:124 | ||||
| chrX:18354672-18354783 | Common:1; Rare:26 | ||||
| chrX:18984017-18984211 | Rare:44 | ||||
| chrX:19343701-19344018 | Common:6; Rare:88; Clinvar (benign):1 | ||||
| chrX:21374157-21374448 | Rare:62 | ||||
| chrX:21839528-21839696 | Rare:41 | ||||
| chrX:21940385-21940834 | Common:3; Rare:107 | ||||
| chrX:23667316-23667602 | Common:2; Rare:88 | ||||
| chrX:23782940-23783342 | Common:5; Rare:84 |