| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:111410045-111410704 | Rare:72; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
| chrX:111410898-111411050 | Rare:33 | ||||
| chrX:111681014-111681331 | Rare:84; Clinvar (benign):7 | ||||
| chrX:112840468-112840529 | Rare:8 | ||||
| chrX:112840868-112841055 | Rare:33 | ||||
| chrX:117972760-117973180 | Common:2; Rare:70 | ||||
| chrX:117973187-117973232 | Rare:3 | ||||
| chrX:117973349-117973845 | Common:2; Rare:66 | ||||
| chrX:117973914-117973917 | |||||
| chrX:118345886-118346180 | Common:3; Rare:53 | ||||
| chrX:118346393-118346495 | Rare:23 | ||||
| chrX:119236133-119236352 | Rare:55 | ||||
| chrX:119236514-119236670 | Rare:44 | ||||
| chrX:119468209-119468518 | Common:3; Rare:102 | ||||
| chrX:119469068-119469330 | Rare:70 |