| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:54357989-54358230 | Common:1; Rare:38 | ||||
| chrX:54530046-54530305 | Common:2; Rare:38 | ||||
| chrX:63351314-63351560 | Common:1; Rare:59 | ||||
| chrX:63785159-63785313 | Rare:35 | ||||
| chrX:65034708-65034899 | Common:1; Rare:37 | ||||
| chrX:65667447-65667753 | Common:1; Rare:60 | ||||
| chrX:68828836-68829030 | Rare:38 | ||||
| chrX:70289879-70290073 | Rare:40 | ||||
| chrX:70931094-70931215 | Common:2; Rare:10 | ||||
| chrX:71532845-71533111 | Rare:50 | ||||
| chrX:73563031-73563230 | Common:1; Rare:29 | ||||
| chrX:75523018-75523144 | Rare:28 | ||||
| chrX:77895417-77895750 | Rare:90; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:79367307-79367471 | Common:1; Rare:33 | ||||
| chrX:81201887-81202179 | Rare:49 |