| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:12975762-12976150 | Common:4; Rare:65 | ||||
| chrX:12976155-12976203 | Rare:9 | ||||
| chrX:13652991-13653312 | Common:2; Rare:73 | ||||
| chrX:13734449-13734859 | Common:3; Rare:116; Clinvar (benign):1 | ||||
| chrX:13817256-13817483 | Common:1; Rare:43 | ||||
| chrX:13938609-13938945 | Common:1; Rare:65 | ||||
| chrX:14029792-14030020 | Common:2; Rare:65 | ||||
| chrX:14529424-14529589 | Common:1; Rare:22 | ||||
| chrX:14873228-14873495 | Rare:43 | ||||
| chrX:15335509-15335835 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chrX:15790394-15790871 | Common:2; Rare:96 | ||||
| chrX:16712356-16712491 | Rare:19 | ||||
| chrX:16719361-16719716 | Rare:93 | ||||
| chrX:16786341-16786573 | Common:1; Rare:59 | ||||
| chrX:16869724-16870034 | Common:3; Rare:61 |