| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103686653-103687324 | Common:5; Rare:108 | ||||
| chrX:103687996-103688379 | Common:1; Rare:47 | ||||
| chrX:104156886-104157069 | Common:1; Rare:29 | ||||
| chrX:106726567-106726929 | Common:1; Rare:83 | ||||
| chrX:107118563-107118897 | Common:3; Rare:62 | ||||
| chrX:107628219-107628528 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chrX:107716279-107716849 | Common:1; Rare:96 | ||||
| chrX:107716902-107717193 | Common:2; Rare:35 | ||||
| chrX:107775581-107775866 | Rare:45 | ||||
| chrX:107775877-107776011 | Common:1; Rare:16 | ||||
| chrX:107825851-107825903 | Rare:7 | ||||
| chrX:108091511-108091822 | Rare:82 | ||||
| chrX:108439492-108439853 | Common:2; Rare:84 | ||||
| chrX:108736366-108736561 | Rare:30 | ||||
| chrX:109733150-109733355 | Common:1; Rare:50 |