| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:13652983-13653169 | Rare:42 | ||||
| chrX:13734526-13734849 | Common:3; Rare:98; Clinvar (benign):1 | ||||
| chrX:14873034-14873488 | Common:1; Rare:84 | ||||
| chrX:15790415-15790566 | Rare:35 | ||||
| chrX:15854717-15854915 | Rare:43 | ||||
| chrX:16719279-16719683 | Rare:97 | ||||
| chrX:16870406-16870752 | Common:1; Rare:80 | ||||
| chrX:18984136-18984200 | Rare:13 | ||||
| chrX:19343701-19343997 | Common:6; Rare:83 | ||||
| chrX:21374145-21374418 | Rare:58 | ||||
| chrX:21839490-21839663 | Rare:39 | ||||
| chrX:21940649-21940764 | Common:1; Rare:28 | ||||
| chrX:23667340-23667573 | Common:2; Rare:76 | ||||
| chrX:23783036-23783334 | Common:4; Rare:55 | ||||
| chrX:23907714-23908006 | Common:1; Rare:60 |