| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:11111135-11111359 | Common:3; Rare:49 | ||||
| chrX:11759443-11759647 | Rare:26 | ||||
| chrX:12975005-12975285 | Common:2; Rare:65 | ||||
| chrX:13688969-13689207 | Common:1; Rare:64 | ||||
| chrX:13734540-13734849 | Common:3; Rare:94; Clinvar (benign):1 | ||||
| chrX:14873228-14873474 | Rare:40 | ||||
| chrX:15493212-15493408 | Common:1; Rare:35 | ||||
| chrX:15790394-15790504 | Rare:31 | ||||
| chrX:19670887-19670968 | Rare:15 | ||||
| chrX:23667280-23667599 | Common:3; Rare:95 | ||||
| chrX:23743238-23743612 | Common:8; Rare:66 | ||||
| chrX:23782860-23783375 | Common:6; Rare:105 | ||||
| chrX:23907714-23907792 | Common:1; Rare:18 | ||||
| chrX:24054890-24054992 | Rare:39 | ||||
| chrX:37847511-37847677 | Common:1; Rare:42 |