| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:75156268-75156315 | Common:1; Rare:11 | ||||
| chrX:75273886-75274130 | Rare:37 | ||||
| chrX:77786198-77786315 | Common:1; Rare:14 | ||||
| chrX:77895417-77895741 | Rare:89; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77910508-77910745 | Common:1; Rare:39 | ||||
| chrX:78103899-78104282 | Common:4; Rare:128 | ||||
| chrX:78139667-78139765 | Common:2; Rare:21 | ||||
| chrX:78945180-78945410 | Rare:27 | ||||
| chrX:81121628-81121870 | Common:2; Rare:38 | ||||
| chrX:81201719-81201832 | Rare:6 | ||||
| chrX:81201911-81202169 | Rare:45 | ||||
| chrX:86047531-86047604 | Common:1; Rare:16 | ||||
| chrX:96684682-96684914 | Rare:48 | ||||
| chrX:100820268-100820417 | Common:2; Rare:30 | ||||
| chrX:101051862-101051930 | Common:1; Rare:13 |