| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75523163-75523307 | Common:1; Rare:22 | ||||
| chrX:77895395-77895729 | Rare:96; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chrX:78103951-78104310 | Common:4; Rare:131 | ||||
| chrX:78139612-78139745 | Common:2; Rare:60 | ||||
| chrX:81201897-81202242 | Rare:60 | ||||
| chrX:93673562-93673744 | Common:1; Rare:28 | ||||
| chrX:100643960-100644279 | Common:1; Rare:43 | ||||
| chrX:101052053-101052222 | Rare:22 | ||||
| chrX:101407893-101408292 | Common:5; Rare:73; Clinvar:1; Clinvar (benign):10 | ||||
| chrX:101418223-101418378 | Common:2; Rare:24 | ||||
| chrX:102142403-102142582 | Rare:45 | ||||
| chrX:102651303-102651541 | Common:2; Rare:65 | ||||
| chrX:103376427-103376612 | Common:1; Rare:27 | ||||
| chrX:103585455-103585863 | Common:3; Rare:85 | ||||
| chrX:103607689-103608073 | Common:1; Rare:62 |