| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:106611679-106612014 | Rare:65 | ||||
| chrX:106612401-106612986 | Rare:171 | ||||
| chrX:106726567-106726727 | Rare:39 | ||||
| chrX:106802440-106802730 | Common:1; Rare:56 | ||||
| chrX:107000206-107000422 | Rare:31 | ||||
| chrX:107118569-107118915 | Common:3; Rare:64 | ||||
| chrX:107628165-107628574 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chrX:107716350-107716690 | Common:1; Rare:48 | ||||
| chrX:107717044-107717185 | Rare:23 | ||||
| chrX:107775772-107776172 | Common:5; Rare:71 | ||||
| chrX:107825857-107826974 | Common:2; Rare:276 | ||||
| chrX:108091495-108091818 | Rare:89 | ||||
| chrX:108439453-108439891 | Common:3; Rare:98 | ||||
| chrX:108440164-108440395 | Common:2; Rare:47 | ||||
| chrX:109536478-109536641 | Common:2; Rare:21 |