| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54440271-54440481 | Rare:49 | ||||
| chrX:54530042-54530294 | Common:2; Rare:35 | ||||
| chrX:55000194-55000422 | Common:1; Rare:53 | ||||
| chrX:55161108-55161269 | Rare:45 | ||||
| chrX:57121497-57121612 | Common:1; Rare:26 | ||||
| chrX:64205697-64205977 | Common:1; Rare:51 | ||||
| chrX:68433814-68434050 | Common:2; Rare:28 | ||||
| chrX:68498968-68499056 | Rare:22 | ||||
| chrX:70289881-70290099 | Rare:40 | ||||
| chrX:71365937-71366256 | Common:3; Rare:58 | ||||
| chrX:75156239-75156369 | Common:2; Rare:40 | ||||
| chrX:78104004-78104310 | Common:4; Rare:110 | ||||
| chrX:81201904-81202192 | Rare:51 | ||||
| chrX:100928899-100929006 | Common:1; Rare:16 | ||||
| chrX:101407878-101408292 | Common:5; Rare:76; Clinvar:1; Clinvar (benign):10 |