| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48508854-48509029 | Rare:36 | ||||
| chrX:48574880-48574971 | Rare:27 | ||||
| chrX:48597372-48597556 | Rare:28 | ||||
| chrX:48911637-48911743 | Rare:24; Clinvar (benign):3 | ||||
| chrX:48958317-48958432 | Rare:35 | ||||
| chrX:49002196-49002317 | Rare:36 | ||||
| chrX:49073995-49074183 | Rare:46 | ||||
| chrX:49079854-49079946 | Rare:15 | ||||
| chrX:49200151-49200340 | Rare:50; Clinvar:1 | ||||
| chrX:49922353-49922718 | Common:1; Rare:80 | ||||
| chrX:50067462-50067631 | Rare:24; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:51893288-51893754 | Common:2; Rare:89 | ||||
| chrX:53422632-53422927 | Common:1; Rare:71 | ||||
| chrX:53434346-53434471 | Common:1; Rare:30 | ||||
| chrX:53686250-53686525 | Common:1; Rare:47 |