| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56729440-56729559 | Common:1; Rare:14 | ||||
| chrX:64205690-64205977 | Common:1; Rare:51 | ||||
| chrX:65034708-65034849 | Common:1; Rare:30 | ||||
| chrX:68498951-68499059 | Rare:23 | ||||
| chrX:68828837-68829087 | Common:1; Rare:48 | ||||
| chrX:70289872-70290099 | Rare:42 | ||||
| chrX:74614458-74614833 | Common:1; Rare:84 | ||||
| chrX:75156277-75156369 | Common:2; Rare:24 | ||||
| chrX:75273990-75274130 | Rare:22 | ||||
| chrX:77786152-77786318 | Common:1; Rare:24 | ||||
| chrX:77895412-77895726 | Rare:87; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103988-78104356 | Common:4; Rare:131 | ||||
| chrX:81201876-81202203 | Rare:53 | ||||
| chrX:86047516-86047642 | Common:1; Rare:25 | ||||
| chrX:87517605-87518133 | Common:3; Rare:110 |