| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132023108-132023357 | Rare:107 | ||||
| chrX:132217920-132218410 | Rare:92 | ||||
| chrX:132488877-132489399 | Rare:143 | ||||
| chrX:132489828-132490286 | Common:2; Rare:177 | ||||
| chrX:133985109-133985396 | Rare:59; Clinvar:2; Clinvar (benign):5 | ||||
| chrX:133985398-133985816 | Common:1; Rare:84; Clinvar (benign):3 | ||||
| chrX:133985850-133986104 | Rare:55 | ||||
| chrX:134373122-134373415 | Common:8; Rare:127 | ||||
| chrX:134459858-134460315 | Common:7; Rare:169 | ||||
| chrX:134915198-134915408 | Common:1; Rare:31 | ||||
| chrX:135032152-135032383 | Common:1; Rare:86 | ||||
| chrX:135343979-135344231 | Common:2; Rare:73 | ||||
| chrX:135344601-135344861 | Common:2; Rare:86 | ||||
| chrX:135973702-135973808 | Rare:39 | ||||
| chrX:135985329-135985520 | Rare:54; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |