| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:63754656-63754864 | Rare:25 | ||||
| chrX:63755031-63755299 | Rare:58 | ||||
| chrX:64205663-64205961 | Common:1; Rare:52 | ||||
| chrX:65034698-65034859 | Common:1; Rare:33 | ||||
| chrX:65667549-65667749 | Rare:37 | ||||
| chrX:68433440-68433580 | Rare:23 | ||||
| chrX:68498965-68499057 | Rare:22 | ||||
| chrX:70289875-70290112 | Rare:44 | ||||
| chrX:71068402-71068757 | Common:3; Rare:70 | ||||
| chrX:71118462-71118748 | Common:1; Rare:57; Clinvar (benign):2 | ||||
| chrX:71254542-71254831 | Common:1; Rare:27 | ||||
| chrX:71255247-71255337 | Rare:14 | ||||
| chrX:71532894-71533161 | Rare:53 | ||||
| chrX:72181556-72181802 | Common:2; Rare:68 | ||||
| chrX:73214690-73215009 | Common:1; Rare:48 |