| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:53536148-53536513 | Common:3; Rare:60; Clinvar (benign):1 | ||||
| chrX:53683807-53684233 | Common:1; Rare:96 | ||||
| chrX:54043926-54044039 | Rare:22 | ||||
| chrX:54357866-54358151 | Rare:53 | ||||
| chrX:54440271-54440459 | Rare:41 | ||||
| chrX:54530040-54530335 | Common:2; Rare:42 | ||||
| chrX:55000194-55000390 | Rare:38 | ||||
| chrX:55160954-55161239 | Common:2; Rare:71 | ||||
| chrX:56995494-56995643 | Common:1; Rare:30 | ||||
| chrX:57121461-57121606 | Common:1; Rare:35 | ||||
| chrX:64205682-64206011 | Common:1; Rare:58 | ||||
| chrX:65034698-65034859 | Common:1; Rare:33 | ||||
| chrX:67543861-67544065 | Rare:34 | ||||
| chrX:68498965-68499099 | Rare:34 | ||||
| chrX:68828837-68829030 | Rare:38 |