| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107717011-107717340 | Common:1; Rare:32 | ||||
| chrX:107775742-107775958 | Rare:42 | ||||
| chrX:108091521-108091818 | Rare:79 | ||||
| chrX:109733178-109733363 | Common:1; Rare:45 | ||||
| chrX:110318072-110318248 | Rare:44 | ||||
| chrX:111681106-111681294 | Rare:54; Clinvar (benign):7 | ||||
| chrX:111681552-111681630 | Rare:31 | ||||
| chrX:115561017-115561205 | Rare:24 | ||||
| chrX:118345908-118346180 | Common:3; Rare:51 | ||||
| chrX:118726889-118727209 | Rare:40 | ||||
| chrX:119399574-119399609 | Rare:3 | ||||
| chrX:119468209-119468612 | Common:3; Rare:113 | ||||
| chrX:119574356-119574599 | Rare:54 | ||||
| chrX:119791590-119791716 | Rare:50 | ||||
| chrX:119871568-119872013 | Common:3; Rare:86; Clinvar (benign):4 |