| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:40735716-40736034 | Common:2; Rare:111 | ||||
| chrX:41085194-41085848 | Common:6; Rare:273 | ||||
| chrX:41333164-41333657 | Rare:198 | ||||
| chrX:41334011-41334198 | Common:2; Rare:46 | ||||
| chrX:41334148-41334447 | Common:4; Rare:89 | ||||
| chrX:41334460-41334647 | Common:2; Rare:128 | ||||
| chrX:41334954-41335102 | Rare:22 | ||||
| chrX:41335014-41335127 | Common:1; Rare:12 | ||||
| chrX:41923425-41924000 | Common:8; Rare:214 | ||||
| chrX:44542777-44543034 | Common:2; Rare:98 | ||||
| chrX:44872808-44873314 | Common:2; Rare:137 | ||||
| chrX:44873290-44873648 | Common:2; Rare:136; Clinvar (benign):3 | ||||
| chrX:46447148-46447369 | Rare:76 | ||||
| chrX:46545358-46545581 | Common:1; Rare:88; Clinvar (benign):1 | ||||
| chrX:46759078-46759340 | Common:1; Rare:91 |