| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129843715-129843734 | Rare:2 | ||||
| chrX:130110483-130110677 | Common:1; Rare:42 | ||||
| chrX:130165652-130165954 | Rare:60; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339789-130339979 | Rare:26 | ||||
| chrX:132218083-132218286 | Rare:24 | ||||
| chrX:134797073-134797251 | Rare:37 | ||||
| chrX:134807037-134807266 | Rare:43 | ||||
| chrX:134990895-134991431 | Common:1; Rare:88 | ||||
| chrX:135022455-135022663 | Rare:52 | ||||
| chrX:135032173-135032419 | Rare:58 | ||||
| chrX:135052071-135052252 | Common:1; Rare:59 | ||||
| chrX:135344082-135344215 | Common:1; Rare:20 | ||||
| chrX:135344573-135344855 | Common:2; Rare:53 | ||||
| chrX:135973601-135973835 | Rare:71 | ||||
| chrX:136169610-136169854 | Rare:40 |