| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847471-37847677 | Common:1; Rare:48 | ||||
| chrX:38327465-38327674 | Rare:48 | ||||
| chrX:38561256-38561564 | Common:3; Rare:83; Clinvar (benign):1 | ||||
| chrX:38570518-38570630 | Common:1; Rare:6 | ||||
| chrX:38801231-38801476 | Common:1; Rare:48 | ||||
| chrX:40580698-40581041 | Common:5; Rare:78; Clinvar (benign):3 | ||||
| chrX:40735327-40735664 | Rare:90 | ||||
| chrX:40735794-40736024 | Common:1; Rare:46 | ||||
| chrX:41085715-41085886 | Rare:39 | ||||
| chrX:41333164-41333618 | Rare:99 | ||||
| chrX:41333810-41334000 | Common:2; Rare:48 | ||||
| chrX:43656086-43656322 | Rare:48 | ||||
| chrX:44542780-44543080 | Common:1; Rare:65 | ||||
| chrX:46447171-46447338 | Rare:31 | ||||
| chrX:46545377-46545583 | Common:1; Rare:47; Clinvar (benign):1 |