| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54440240-54440489 | Rare:53 | ||||
| chrX:54530033-54530340 | Common:2; Rare:47 | ||||
| chrX:55000194-55000400 | Rare:42 | ||||
| chrX:56563463-56563654 | Rare:40; Clinvar:1 | ||||
| chrX:56995446-56995632 | Common:1; Rare:42 | ||||
| chrX:57121533-57121585 | Rare:9 | ||||
| chrX:63351274-63351569 | Common:2; Rare:70 | ||||
| chrX:63785128-63785304 | Rare:40; Clinvar (pathogenic):1 | ||||
| chrX:65034705-65034836 | Common:1; Rare:27 | ||||
| chrX:65534708-65534938 | Common:2; Rare:63 | ||||
| chrX:68433819-68433987 | Rare:19 | ||||
| chrX:68498917-68499069 | Rare:33 | ||||
| chrX:68693466-68693644 | Rare:40 | ||||
| chrX:70289903-70290122 | Rare:39 | ||||
| chrX:70931072-70931181 | Rare:11 |