| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55161108-55161269 | Rare:45 | ||||
| chrX:56563522-56563651 | Rare:29; Clinvar:1 | ||||
| chrX:65034723-65034838 | Common:1; Rare:22 | ||||
| chrX:65534734-65534811 | Common:2; Rare:29 | ||||
| chrX:70289888-70290146 | Rare:47 | ||||
| chrX:75156277-75156370 | Common:2; Rare:24 | ||||
| chrX:75523001-75523212 | Common:1; Rare:44 | ||||
| chrX:77895417-77895739 | Rare:87; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:78103929-78104282 | Common:4; Rare:120 | ||||
| chrX:81201911-81202197 | Rare:52 | ||||
| chrX:101407966-101408282 | Common:2; Rare:47; Clinvar (benign):2 | ||||
| chrX:103310910-103311046 | Common:2; Rare:20 | ||||
| chrX:103330084-103330287 | Rare:28 | ||||
| chrX:103356277-103356580 | Common:4; Rare:44 | ||||
| chrX:103585434-103585613 | Common:3; Rare:36 |