| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:7927695-7927770 | Rare:13 | ||||
| chrX:10620419-10620690 | Common:1; Rare:42 | ||||
| chrX:11111136-11111344 | Common:3; Rare:42 | ||||
| chrX:11427728-11427915 | Rare:41 | ||||
| chrX:11665100-11665355 | Rare:42 | ||||
| chrX:12975813-12976150 | Common:4; Rare:58 | ||||
| chrX:13689023-13689242 | Common:2; Rare:65 | ||||
| chrX:13734540-13734854 | Common:3; Rare:95; Clinvar (benign):1 | ||||
| chrX:14029792-14029984 | Common:2; Rare:60 | ||||
| chrX:14873040-14873470 | Common:1; Rare:80 | ||||
| chrX:15335470-15335736 | Common:4; Rare:60; Clinvar (benign):4 | ||||
| chrX:15493220-15493417 | Common:1; Rare:35 | ||||
| chrX:15500583-15500807 | Common:1; Rare:34 | ||||
| chrX:15790421-15790558 | Rare:33 | ||||
| chrX:16719444-16719751 | Rare:87 |