| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:74614440-74614649 | Rare:37 | ||||
| chrX:75156268-75156369 | Common:2; Rare:26 | ||||
| chrX:75274474-75274692 | Common:2; Rare:43 | ||||
| chrX:75523009-75523212 | Common:1; Rare:42 | ||||
| chrX:75523246-75523497 | Common:2; Rare:38 | ||||
| chrX:76172943-76173154 | Rare:51 | ||||
| chrX:77895412-77895689 | Rare:77; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103950-78104289 | Common:4; Rare:117 | ||||
| chrX:80335349-80335407 | Common:1; Rare:8 | ||||
| chrX:81121602-81121870 | Common:2; Rare:43 | ||||
| chrX:81201876-81202199 | Rare:53 | ||||
| chrX:85243726-85244002 | Common:2; Rare:48 | ||||
| chrX:87517722-87518057 | Common:2; Rare:74 | ||||
| chrX:91434814-91434846 | Rare:7 | ||||
| chrX:93673558-93673744 | Common:1; Rare:28 |