| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:138216967-138217288 | Common:2; Rare:82 | ||||
| chrX:2609154-2609444 | Common:1; Rare:93 | ||||
| chrX:2824026-2824267 | Common:3; Rare:39 | ||||
| chrX:5726072-5726182 | Rare:29 | ||||
| chrX:11114693-11114940 | Common:1; Rare:49; Clinvar (pathogenic):1 | ||||
| chrX:11351661-11351732 | Rare:7 | ||||
| chrX:11351735-11351854 | Common:2; Rare:16 | ||||
| chrX:12973790-12973891 | Common:1; Rare:15 | ||||
| chrX:15674804-15675001 | Rare:42 | ||||
| chrX:15675350-15675478 | Common:4; Rare:21 | ||||
| chrX:15675563-15675744 | Common:1; Rare:39 | ||||
| chrX:24025659-24025789 | Rare:29 | ||||
| chrX:38870570-38870771 | Common:4; Rare:31 | ||||
| chrX:40171826-40171919 | Rare:23 | ||||
| chrX:41010140-41010413 | Common:2; Rare:33 |