| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961472-123961812 | Rare:46 | ||||
| chrX:129779848-129779975 | Rare:21 | ||||
| chrX:129906089-129906213 | Rare:26 | ||||
| chrX:130165688-130165918 | Rare:44; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:132023138-132023336 | Rare:50 | ||||
| chrX:132217735-132218012 | Common:1; Rare:36 | ||||
| chrX:132218093-132218297 | Rare:27 | ||||
| chrX:132489036-132489098 | Rare:11 | ||||
| chrX:135022468-135022774 | Rare:63 | ||||
| chrX:135344016-135344240 | Common:1; Rare:40 | ||||
| chrX:135344653-135344828 | Rare:35 | ||||
| chrX:135973695-135973827 | Rare:50 | ||||
| chrX:136196485-136196838 | Rare:54 | ||||
| chrX:136196844-136197133 | Rare:56 | ||||
| chrX:141177041-141177320 | Common:1; Rare:42 |