| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55000194-55000400 | Rare:42 | ||||
| chrX:55161056-55161249 | Rare:58 | ||||
| chrX:56232286-56232395 | Rare:18 | ||||
| chrX:56563431-56563674 | Rare:52; Clinvar:1 | ||||
| chrX:56563901-56564214 | Common:1; Rare:56; Clinvar (benign):1 | ||||
| chrX:56729462-56729578 | Common:1; Rare:15 | ||||
| chrX:56995456-56995608 | Common:1; Rare:35 | ||||
| chrX:57121422-57121627 | Common:1; Rare:48 | ||||
| chrX:64205682-64206021 | Common:1; Rare:63 | ||||
| chrX:65034698-65034899 | Common:1; Rare:38 | ||||
| chrX:66039942-66040155 | Common:1; Rare:51 | ||||
| chrX:66639025-66639223 | Rare:12 | ||||
| chrX:68433373-68433565 | Rare:26 | ||||
| chrX:68498961-68499059 | Rare:22 | ||||
| chrX:68828836-68829077 | Common:1; Rare:46 |