| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:70289858-70290095 | Rare:42 | ||||
| chrX:71254077-71254270 | Common:2; Rare:32 | ||||
| chrX:75156222-75156368 | Common:2; Rare:45 | ||||
| chrX:75274489-75274736 | Common:2; Rare:49 | ||||
| chrX:77895418-77895731 | Rare:83; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78104017-78104289 | Common:4; Rare:94 | ||||
| chrX:81201911-81202167 | Rare:45 | ||||
| chrX:93673546-93673762 | Common:1; Rare:35 | ||||
| chrX:101407841-101408307 | Common:5; Rare:89; Clinvar:2; Clinvar (benign):11 | ||||
| chrX:102712391-102712486 | Common:1; Rare:19 | ||||
| chrX:103356232-103356553 | Common:2; Rare:51 | ||||
| chrX:103586473-103586678 | Rare:41 | ||||
| chrX:104156948-104157058 | Common:1; Rare:18 | ||||
| chrX:107118798-107118894 | Common:2; Rare:17 | ||||
| chrX:108091424-108091815 | Rare:103 |