| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:37847506-37847677 | Common:1; Rare:43 | ||||
| chrX:38327450-38327637 | Rare:43 | ||||
| chrX:40580700-40581004 | Common:4; Rare:67 | ||||
| chrX:40735783-40735847 | Rare:21 | ||||
| chrX:40735850-40736034 | Common:1; Rare:30 | ||||
| chrX:41333158-41333294 | Rare:38 | ||||
| chrX:41333396-41333698 | Rare:53 | ||||
| chrX:41333908-41334297 | Common:4; Rare:100 | ||||
| chrX:41334516-41334663 | Rare:62 | ||||
| chrX:41334993-41335130 | Common:1; Rare:17 | ||||
| chrX:43656104-43656413 | Rare:58 | ||||
| chrX:43973341-43973439 | Rare:4 | ||||
| chrX:43973450-43973581 | Common:1; Rare:23; Clinvar (benign):1 | ||||
| chrX:46545377-46545534 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chrX:46573647-46573837 | Common:1; Rare:29 |