| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123733005-123733149 | Rare:23; Clinvar (benign):1 | ||||
| chrX:123859690-123860114 | Common:2; Rare:62 | ||||
| chrX:123960350-123960752 | Rare:31 | ||||
| chrX:123961264-123961435 | Common:2; Rare:22 | ||||
| chrX:123961546-123961856 | Rare:44 | ||||
| chrX:123961979-123962110 | Rare:19 | ||||
| chrX:129779775-129779989 | Rare:35 | ||||
| chrX:129905916-129906232 | Rare:80 | ||||
| chrX:130165616-130165937 | Rare:66; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339786-130339962 | Rare:25 | ||||
| chrX:130401868-130402029 | Common:2; Rare:50 | ||||
| chrX:132023135-132023336 | Rare:51 | ||||
| chrX:132217933-132218291 | Rare:45 | ||||
| chrX:132219424-132219513 | Rare:7 | ||||
| chrX:132413544-132413853 | Rare:44 |