| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107715741-107716045 | Common:1; Rare:44 | ||||
| chrX:107716088-107716114 | Rare:2 | ||||
| chrX:107716142-107717088 | Common:3; Rare:150 | ||||
| chrX:107775610-107776181 | Common:4; Rare:91 | ||||
| chrX:108091512-108091825 | Rare:83 | ||||
| chrX:108439457-108440022 | Common:3; Rare:121 | ||||
| chrX:109733161-109733470 | Common:1; Rare:69 | ||||
| chrX:110317883-110318248 | Rare:95 | ||||
| chrX:111680984-111681296 | Rare:78; Clinvar (benign):7 | ||||
| chrX:111681558-111681636 | Rare:31 | ||||
| chrX:115560747-115561102 | Common:2; Rare:58 | ||||
| chrX:115561112-115561244 | Common:1; Rare:26 | ||||
| chrX:118345859-118346176 | Common:3; Rare:56 | ||||
| chrX:118346477-118346495 | Rare:4 | ||||
| chrX:119399342-119399530 | Common:2; Rare:35 |