| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48475880-48476209 | Rare:52 | ||||
| chrX:48508861-48509026 | Rare:31 | ||||
| chrX:48696529-48696765 | Common:1; Rare:52 | ||||
| chrX:53422637-53422920 | Common:1; Rare:67 | ||||
| chrX:55000204-55000385 | Rare:34 | ||||
| chrX:55161164-55161256 | Rare:22 | ||||
| chrX:65034711-65034901 | Common:1; Rare:37 | ||||
| chrX:68498984-68499056 | Rare:16 | ||||
| chrX:70289879-70290105 | Rare:42 | ||||
| chrX:77895423-77895741 | Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201911-81202128 | Rare:40 | ||||
| chrX:101407897-101408214 | Common:5; Rare:59; Clinvar (benign):9 | ||||
| chrX:108091529-108091810 | Rare:74 | ||||
| chrX:109733289-109733559 | Common:1; Rare:53 | ||||
| chrX:119468365-119468506 | Common:1; Rare:57 |