| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11111202-11111356 | Common:3; Rare:31 | ||||
| chrX:12975005-12975166 | Common:1; Rare:40 | ||||
| chrX:13734551-13734815 | Common:3; Rare:83; Clinvar (benign):1 | ||||
| chrX:14873275-14873463 | Rare:28 | ||||
| chrX:16719518-16719677 | Rare:48 | ||||
| chrX:24054884-24054987 | Rare:37 | ||||
| chrX:24149629-24149744 | Rare:22 | ||||
| chrX:46545393-46545520 | Rare:22 | ||||
| chrX:47144654-47144837 | Common:1; Rare:30 | ||||
| chrX:47144965-47145295 | Rare:43 | ||||
| chrX:48071629-48071819 | Common:1; Rare:28 | ||||
| chrX:48468294-48468491 | Common:1; Rare:25 | ||||
| chrX:49079858-49079946 | Rare:15 | ||||
| chrX:53422632-53422918 | Common:1; Rare:71 | ||||
| chrX:54440271-54440421 | Rare:25 |