| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129779817-129779971 | Rare:21 | ||||
| chrX:129906053-129906193 | Rare:39 | ||||
| chrX:130171836-130171992 | Common:1; Rare:40 | ||||
| chrX:132023144-132023305 | Rare:41 | ||||
| chrX:135052096-135052344 | Common:2; Rare:71 | ||||
| chrX:135344597-135344812 | Common:2; Rare:38 | ||||
| chrX:135973698-135973797 | Rare:35 | ||||
| chrX:136147250-136147566 | Common:3; Rare:38 | ||||
| chrX:138711256-138711494 | Common:2; Rare:57 | ||||
| chrX:141177076-141177321 | Common:1; Rare:33 | ||||
| chrX:149938451-149938626 | Rare:43 | ||||
| chrX:151397102-151397263 | Common:2; Rare:69 | ||||
| chrX:152830712-152831022 | Common:1; Rare:56 | ||||
| chrX:153494688-153495040 | Common:3; Rare:55 | ||||
| chrX:153794301-153794690 | Common:1; Rare:116; Clinvar (benign):2 |