| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132023142-132023352 | Rare:50 | ||||
| chrX:132218084-132218278 | Rare:21 | ||||
| chrX:134807034-134807275 | Rare:44 | ||||
| chrX:135052110-135052307 | Common:2; Rare:55 | ||||
| chrX:135344688-135344813 | Rare:23 | ||||
| chrX:135973637-135973775 | Rare:37 | ||||
| chrX:136497359-136497628 | Common:1; Rare:62 | ||||
| chrX:141177083-141177317 | Rare:32 | ||||
| chrX:149504254-149504480 | Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
| chrX:149505282-149505446 | Rare:41 | ||||
| chrX:149540771-149541117 | Common:4; Rare:63 | ||||
| chrX:149938390-149938652 | Common:2; Rare:65 | ||||
| chrX:151397042-151397248 | Common:4; Rare:102 | ||||
| chrX:152830722-152831089 | Common:2; Rare:64 | ||||
| chrX:153599097-153599356 | Common:13; Rare:52 |