| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123960350-123960748 | Rare:28 | ||||
| chrX:123961206-123961432 | Common:2; Rare:31 | ||||
| chrX:123961540-123961850 | Rare:44 | ||||
| chrX:129843808-129844003 | Rare:26 | ||||
| chrX:129906051-129906216 | Rare:44 | ||||
| chrX:129982428-129982638 | Common:1; Rare:31 | ||||
| chrX:130165703-130165908 | Rare:40; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130171850-130172039 | Common:1; Rare:49 | ||||
| chrX:130339795-130339991 | Rare:31 | ||||
| chrX:130401873-130402040 | Common:2; Rare:49 | ||||
| chrX:132218040-132218248 | Rare:14 | ||||
| chrX:134373142-134373421 | Common:4; Rare:62 | ||||
| chrX:135022468-135022561 | Rare:32 | ||||
| chrX:135032223-135032378 | Rare:36 | ||||
| chrX:135032867-135032992 | Rare:18 |