| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:56232302-56232458 | Rare:22 | ||||
| chrX:56232803-56232910 | Common:1; Rare:10 | ||||
| chrX:56729485-56729530 | Rare:5 | ||||
| chrX:57121418-57121653 | Common:1; Rare:55 | ||||
| chrX:63755045-63755330 | Rare:61 | ||||
| chrX:64205690-64206021 | Common:1; Rare:62 | ||||
| chrX:65034690-65034865 | Common:1; Rare:35 | ||||
| chrX:65667553-65667844 | Rare:51 | ||||
| chrX:68498961-68499091 | Rare:32 | ||||
| chrX:68647531-68647688 | Common:2; Rare:32 | ||||
| chrX:68693469-68693698 | Rare:57 | ||||
| chrX:68828843-68829034 | Rare:39 | ||||
| chrX:70454883-70455202 | Rare:34 | ||||
| chrX:71111551-71111685 | Rare:16; Clinvar:2 | ||||
| chrX:71118591-71118748 | Rare:36; Clinvar (benign):2 |