| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:24149648-24149778 | Rare:23 | ||||
| chrX:24465044-24465349 | Common:4; Rare:88 | ||||
| chrX:30653088-30653504 | Common:2; Rare:102 | ||||
| chrX:37847471-37847677 | Common:1; Rare:48 | ||||
| chrX:38561264-38561577 | Common:3; Rare:81; Clinvar (benign):1 | ||||
| chrX:40580742-40581051 | Common:5; Rare:74; Clinvar (benign):3 | ||||
| chrX:40735457-40735709 | Rare:72 | ||||
| chrX:41085221-41085385 | Common:2; Rare:36 | ||||
| chrX:41333222-41333529 | Rare:62 | ||||
| chrX:41333857-41334288 | Common:6; Rare:113 | ||||
| chrX:41334603-41334640 | Rare:18 | ||||
| chrX:41688654-41689070 | Common:2; Rare:45 | ||||
| chrX:43656066-43656414 | Rare:62 | ||||
| chrX:46545380-46545564 | Rare:43 | ||||
| chrX:46836984-46837110 | Rare:30; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 |