| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75156258-75156385 | Common:2; Rare:33 | ||||
| chrX:77895404-77895741 | Rare:95; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201911-81202183 | Rare:49 | ||||
| chrX:93673543-93673936 | Common:1; Rare:59 | ||||
| chrX:101407899-101408285 | Common:5; Rare:69; Clinvar (benign):9 | ||||
| chrX:103356275-103356558 | Common:3; Rare:44 | ||||
| chrX:103586437-103586742 | Rare:66 | ||||
| chrX:104156946-104157045 | Common:1; Rare:18 | ||||
| chrX:108091452-108091822 | Rare:97 | ||||
| chrX:118727458-118727711 | Rare:51 | ||||
| chrX:119399000-119399362 | Common:3; Rare:66 | ||||
| chrX:119468205-119468506 | Common:3; Rare:99 | ||||
| chrX:119574382-119574575 | Rare:42 | ||||
| chrX:119871695-119871903 | Common:1; Rare:51; Clinvar (benign):2 | ||||
| chrX:119943709-119943885 | Rare:32 |