| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:106726613-106726741 | Rare:37 | ||||
| chrX:106802520-106802763 | Rare:51 | ||||
| chrX:107118764-107118913 | Common:2; Rare:31 | ||||
| chrX:107628201-107628523 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chrX:107716441-107716565 | Common:1; Rare:22 | ||||
| chrX:107716989-107717167 | Common:1; Rare:23 | ||||
| chrX:108091512-108091822 | Rare:82 | ||||
| chrX:109537065-109537242 | Common:1; Rare:37 | ||||
| chrX:109733150-109733491 | Common:1; Rare:81 | ||||
| chrX:110002342-110002448 | Rare:18 | ||||
| chrX:110317938-110318310 | Rare:109 | ||||
| chrX:111681058-111681312 | Rare:64; Clinvar (benign):7 | ||||
| chrX:111681536-111681749 | Rare:73 | ||||
| chrX:112840815-112841048 | Rare:46 | ||||
| chrX:115560979-115561251 | Common:1; Rare:49 |