| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:134915166-134915494 | Common:1; Rare:51 | ||||
| chrX:135022468-135022574 | Rare:34 | ||||
| chrX:135032170-135032404 | Rare:55 | ||||
| chrX:135032561-135032901 | Rare:61 | ||||
| chrX:135052100-135052331 | Common:2; Rare:67 | ||||
| chrX:135344669-135344830 | Rare:35 | ||||
| chrX:135973675-135973896 | Rare:72 | ||||
| chrX:135985311-135985688 | Rare:115; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chrX:136147260-136147618 | Common:4; Rare:49 | ||||
| chrX:136497079-136497439 | Common:3; Rare:93 | ||||
| chrX:136880595-136880776 | Common:1; Rare:45 | ||||
| chrX:136880779-136880920 | Rare:32 | ||||
| chrX:137566442-137566683 | Rare:36 | ||||
| chrX:138711183-138711469 | Common:2; Rare:67 | ||||
| chrX:138711652-138711814 | Common:2; Rare:31 |