| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:142205217-142205343 | Common:1; Rare:29 | ||||
| chrX:143720742-143720925 | Common:2; Rare:43 | ||||
| chrX:147911765-147911790 | Rare:6 | ||||
| chrX:147911809-147912182 | Common:3; Rare:119 | ||||
| chrX:147981236-147981377 | Rare:28 | ||||
| chrX:148718954-148719097 | Rare:10 | ||||
| chrX:149540409-149540584 | Common:2; Rare:16 | ||||
| chrX:149540724-149541048 | Common:5; Rare:65 | ||||
| chrX:149631677-149631859 | Common:1; Rare:60 | ||||
| chrX:149938407-149938667 | Common:2; Rare:65 | ||||
| chrX:150568328-150568716 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chrX:150693282-150693399 | Common:1; Rare:28 | ||||
| chrX:150898584-150898916 | Common:3; Rare:94 | ||||
| chrX:150980410-150980578 | Rare:17 | ||||
| chrX:151397014-151397320 | Common:6; Rare:146 |