| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:74614483-74614804 | Common:1; Rare:74 | ||||
| chrX:75156268-75156305 | Common:1; Rare:9 | ||||
| chrX:75274610-75274733 | Common:2; Rare:24 | ||||
| chrX:76172719-76173148 | Rare:77 | ||||
| chrX:77895412-77895731 | Rare:87; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201911-81202203 | Rare:52 | ||||
| chrX:101407877-101408307 | Common:5; Rare:80; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:103330116-103330255 | Rare:22 | ||||
| chrX:103356407-103356603 | Common:3; Rare:23 | ||||
| chrX:103376427-103376613 | Common:1; Rare:27 | ||||
| chrX:103585425-103585633 | Common:3; Rare:41 | ||||
| chrX:103629448-103629505 | Rare:14 | ||||
| chrX:104156906-104157069 | Common:1; Rare:28 | ||||
| chrX:107716438-107716565 | Common:1; Rare:22 | ||||
| chrX:107717058-107717222 | Rare:20 |