| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:63755076-63755321 | Rare:55 | ||||
| chrX:64205682-64205977 | Common:1; Rare:52 | ||||
| chrX:65034708-65034859 | Common:1; Rare:32 | ||||
| chrX:67545000-67545362 | Common:1; Rare:78; Clinvar:1 | ||||
| chrX:68498965-68499056 | Rare:22 | ||||
| chrX:68828795-68829025 | Rare:50 | ||||
| chrX:70289888-70290053 | Rare:34 | ||||
| chrX:71068310-71068468 | Common:1; Rare:48 | ||||
| chrX:71118500-71118553 | Common:1; Rare:8 | ||||
| chrX:71118557-71118748 | Rare:41; Clinvar (benign):2 | ||||
| chrX:71254067-71254271 | Common:2; Rare:34 | ||||
| chrX:71283464-71283724 | Rare:43 | ||||
| chrX:71532920-71533145 | Rare:42 | ||||
| chrX:72305872-72306074 | Rare:34 | ||||
| chrX:73563044-73563302 | Common:1; Rare:38 |