| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:123961290-123961322 | Common:2; Rare:14 | ||||
| chrX:123961369-123961433 | Rare:4 | ||||
| chrX:123961540-123961853 | Rare:45 | ||||
| chrX:129523418-129523647 | Common:3; Rare:39 | ||||
| chrX:129843805-129844022 | Common:1; Rare:26 | ||||
| chrX:129906057-129906217 | Rare:42 | ||||
| chrX:130165688-130165916 | Rare:44; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130339780-130339973 | Rare:29 | ||||
| chrX:132023135-132023348 | Rare:51 | ||||
| chrX:132218040-132218282 | Rare:25 | ||||
| chrX:132219439-132219515 | Rare:6 | ||||
| chrX:134373143-134373427 | Common:4; Rare:62 | ||||
| chrX:135032198-135032373 | Rare:36 | ||||
| chrX:135344634-135344823 | Common:1; Rare:35 | ||||
| chrX:135973671-135973870 | Rare:66 |