| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:68498958-68499069 | Rare:27 | ||||
| chrX:70289888-70290112 | Rare:40 | ||||
| chrX:71532875-71533115 | Rare:46 | ||||
| chrX:75156277-75156369 | Common:2; Rare:24 | ||||
| chrX:76173005-76173127 | Rare:32 | ||||
| chrX:77895417-77895741 | Rare:89; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201881-81202197 | Rare:53 | ||||
| chrX:86047516-86047638 | Common:1; Rare:25 | ||||
| chrX:101390862-101391046 | Rare:59 | ||||
| chrX:101407902-101408282 | Common:5; Rare:68; Clinvar (benign):9 | ||||
| chrX:101418214-101418287 | Common:1; Rare:12 | ||||
| chrX:102125573-102125758 | Common:2; Rare:40 | ||||
| chrX:103214989-103215171 | Common:2; Rare:40 | ||||
| chrX:103628990-103629003 | Rare:3 | ||||
| chrX:103629443-103629531 | Rare:25 |