| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129523213-129523283 | Rare:24 | ||||
| chrX:130110447-130110623 | Rare:42 | ||||
| chrX:130165671-130165935 | Rare:51; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023144-132023345 | Rare:49 | ||||
| chrX:132217710-132218012 | Common:1; Rare:40 | ||||
| chrX:132218040-132218282 | Rare:25 | ||||
| chrX:133415491-133415747 | Rare:60 | ||||
| chrX:135022468-135022571 | Rare:33 | ||||
| chrX:135032152-135032386 | Common:1; Rare:56 | ||||
| chrX:135032647-135033048 | Rare:66 | ||||
| chrX:135343999-135344240 | Common:1; Rare:42 | ||||
| chrX:135344625-135344823 | Common:1; Rare:38 | ||||
| chrX:135973695-135973827 | Rare:50 | ||||
| chrX:136169323-136169634 | Common:2; Rare:36 | ||||
| chrX:136206242-136206588 | Rare:53; Clinvar:2; Clinvar (benign):5 |