| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:107716804-107716838 | Rare:7 | ||||
| chrX:107716928-107717234 | Common:2; Rare:36 | ||||
| chrX:108091504-108091822 | Rare:86 | ||||
| chrX:108439457-108439901 | Common:3; Rare:99 | ||||
| chrX:109733158-109733502 | Common:1; Rare:82 | ||||
| chrX:110317931-110318251 | Rare:84 | ||||
| chrX:111681031-111681302 | Rare:70; Clinvar (benign):7 | ||||
| chrX:111681536-111681630 | Rare:36 | ||||
| chrX:112840575-112841095 | Rare:99 | ||||
| chrX:115561100-115561251 | Common:1; Rare:27 | ||||
| chrX:118345805-118346165 | Common:4; Rare:64 | ||||
| chrX:119236556-119236651 | Rare:27 | ||||
| chrX:119468216-119468456 | Common:3; Rare:68 | ||||
| chrX:119574373-119574586 | Rare:47 | ||||
| chrX:119791578-119791978 | Common:2; Rare:108 |