| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:102915810-102915905 | Common:1; Rare:13 | ||||
| chrX:103404669-103404852 | Common:2; Rare:28 | ||||
| chrX:103678782-103679166 | Common:3; Rare:62 | ||||
| chrX:107084335-107084631 | Common:1; Rare:34 | ||||
| chrX:109683759-109683829 | Rare:11 | ||||
| chrX:115719037-115719065 | Rare:8 | ||||
| chrX:115932225-115932480 | Common:4; Rare:33 | ||||
| chrX:115966265-115966483 | Rare:27 | ||||
| chrX:118566592-118566801 | Rare:19 | ||||
| chrX:118687631-118687927 | Rare:37 | ||||
| chrX:119786297-119786515 | Common:3; Rare:24 | ||||
| chrX:120557682-120557929 | Common:1; Rare:38; Clinvar (benign):1 | ||||
| chrX:126472659-126472822 | Common:2; Rare:24 | ||||
| chrX:126473182-126473225 | Common:1; Rare:3 | ||||
| chrX:129515748-129515961 | Rare:33 |