| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:81201889-81202198 | Rare:53 | ||||
| chrX:101407897-101408284 | Common:5; Rare:70; Clinvar (benign):9 | ||||
| chrX:101418202-101418297 | Common:1; Rare:15 | ||||
| chrX:103629448-103629527 | Rare:21 | ||||
| chrX:104156894-104157069 | Common:1; Rare:29 | ||||
| chrX:107118764-107118889 | Common:2; Rare:25 | ||||
| chrX:107716448-107716835 | Common:1; Rare:66 | ||||
| chrX:107716929-107717192 | Common:2; Rare:31 | ||||
| chrX:107775606-107775943 | Rare:58 | ||||
| chrX:108091523-108091822 | Rare:79 | ||||
| chrX:118345861-118346156 | Common:3; Rare:50 | ||||
| chrX:119468238-119468506 | Common:3; Rare:93 | ||||
| chrX:119469090-119469282 | Rare:56 | ||||
| chrX:119574374-119574603 | Rare:52 | ||||
| chrX:119582478-119582676 | Rare:28; Clinvar (benign):1 |