| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53434352-53434523 | Common:1; Rare:39 | ||||
| chrX:55000204-55000385 | Rare:34 | ||||
| chrX:55161108-55161269 | Rare:45 | ||||
| chrX:56729498-56729530 | Rare:3 | ||||
| chrX:57121446-57121599 | Common:1; Rare:37 | ||||
| chrX:65034720-65034823 | Common:1; Rare:22 | ||||
| chrX:70289881-70290130 | Rare:46 | ||||
| chrX:71532839-71533136 | Rare:56 | ||||
| chrX:72238976-72239156 | Rare:48 | ||||
| chrX:76172719-76173086 | Rare:59 | ||||
| chrX:77895417-77895731 | Rare:84; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:81201887-81202175 | Rare:47 | ||||
| chrX:86047531-86047663 | Common:1; Rare:23 | ||||
| chrX:100820282-100820417 | Common:2; Rare:29 | ||||
| chrX:101097894-101098233 | Common:1; Rare:65 |