| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:110002323-110002448 | Rare:22 | ||||
| chrX:110003042-110003129 | Rare:15 | ||||
| chrX:110317877-110318251 | Rare:99 | ||||
| chrX:110944511-110944610 | Rare:14 | ||||
| chrX:111096010-111096194 | Rare:26 | ||||
| chrX:111681106-111681302 | Rare:55; Clinvar (benign):7 | ||||
| chrX:111681535-111681673 | Rare:51 | ||||
| chrX:112840775-112841033 | Rare:54 | ||||
| chrX:115561011-115561244 | Common:1; Rare:42 | ||||
| chrX:115593129-115593332 | Common:1; Rare:21 | ||||
| chrX:115593482-115593611 | Common:1; Rare:18 | ||||
| chrX:116436388-116436624 | Rare:22 | ||||
| chrX:118345875-118346156 | Common:3; Rare:48 | ||||
| chrX:118346352-118346512 | Rare:33 | ||||
| chrX:118974506-118974671 | Rare:30 |