| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:10014930-10015295 | Common:2; Rare:134 | ||||
| chrX:10156690-10157000 | Common:2; Rare:37 | ||||
| chrX:10620458-10620690 | Common:1; Rare:31 | ||||
| chrX:11111103-11111473 | Common:8; Rare:133 | ||||
| chrX:11758033-11758255 | Common:4; Rare:71 | ||||
| chrX:11759280-11759684 | Common:2; Rare:86 | ||||
| chrX:12791294-12791488 | Rare:43 | ||||
| chrX:12974160-12974710 | Common:1; Rare:68 | ||||
| chrX:12975002-12975315 | Common:4; Rare:135 | ||||
| chrX:13652840-13653340 | Common:6; Rare:203 | ||||
| chrX:13653340-13653740 | Common:2; Rare:87 | ||||
| chrX:13688969-13689265 | Common:3; Rare:132 | ||||
| chrX:13689429-13689550 | Common:2; Rare:22 | ||||
| chrX:13734526-13734948 | Common:6; Rare:220; Clinvar (benign):2 | ||||
| chrX:13735013-13735187 | Common:1; Rare:81; Clinvar (benign):2 |