| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:102142358-102142595 | Rare:55 | ||||
| chrX:102471792-102472079 | Rare:7 | ||||
| chrX:102651313-102651554 | Common:2; Rare:62 | ||||
| chrX:102712249-102712454 | Common:1; Rare:53 | ||||
| chrX:102712801-102712901 | Rare:14 | ||||
| chrX:102745648-102745989 | Common:2; Rare:87 | ||||
| chrX:103080931-103081028 | Rare:15 | ||||
| chrX:103083019-103083240 | Rare:37 | ||||
| chrX:103092986-103093340 | Common:1; Rare:55 | ||||
| chrX:103214974-103215235 | Common:2; Rare:52 | ||||
| chrX:103255072-103255349 | Rare:30 | ||||
| chrX:103276677-103276903 | Rare:27 | ||||
| chrX:103310381-103310684 | Common:1; Rare:71; Clinvar (benign):1 | ||||
| chrX:103356277-103356603 | Common:4; Rare:46 | ||||
| chrX:103356852-103357172 | Rare:47 |