| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:145817643-145817943 | Common:2; Rare:51 | ||||
| chrX:149505232-149505382 | Rare:49 | ||||
| chrX:149540789-149541048 | Common:4; Rare:50 | ||||
| chrX:149631731-149631875 | Common:1; Rare:33 | ||||
| chrX:149938440-149938603 | Common:1; Rare:45 | ||||
| chrX:150692674-150692974 | Common:2; Rare:31 | ||||
| chrX:150898539-150898891 | Common:3; Rare:97 | ||||
| chrX:151397054-151397290 | Common:4; Rare:119 | ||||
| chrX:152451220-152451410 | Common:3; Rare:24 | ||||
| chrX:152830688-152831099 | Common:3; Rare:73 | ||||
| chrX:152941509-152941706 | Common:1; Rare:51 | ||||
| chrX:153599076-153599461 | Common:15; Rare:81 | ||||
| chrX:153724347-153724616 | Common:2; Rare:70 | ||||
| chrX:153794268-153794708 | Common:1; Rare:137; Clinvar (benign):2 | ||||
| chrX:153886080-153886291 | Common:1; Rare:35 |