| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11111141-11111356 | Common:3; Rare:45 | ||||
| chrX:11759356-11759657 | Common:1; Rare:41 | ||||
| chrX:12974964-12975168 | Common:2; Rare:53 | ||||
| chrX:12976152-12976361 | Rare:45 | ||||
| chrX:13652977-13653150 | Rare:41 | ||||
| chrX:13734529-13734854 | Common:3; Rare:99; Clinvar (benign):1 | ||||
| chrX:13938603-13938769 | Rare:36 | ||||
| chrX:14529394-14529872 | Common:2; Rare:64 | ||||
| chrX:14873228-14873470 | Rare:39 | ||||
| chrX:15493241-15493509 | Common:1; Rare:39 | ||||
| chrX:16712872-16712980 | Common:1; Rare:10 | ||||
| chrX:16719487-16719690 | Rare:64 | ||||
| chrX:16786175-16786548 | Common:2; Rare:83 | ||||
| chrX:18707560-18707709 | Rare:18 | ||||
| chrX:19343700-19343997 | Common:6; Rare:83 |