| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:46836696-46837111 | Rare:76; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:46912509-46912651 | Rare:38 | ||||
| chrX:47144474-47144843 | Common:2; Rare:80; Clinvar (benign):1 | ||||
| chrX:47144995-47145317 | Rare:41 | ||||
| chrX:47190654-47190917 | Rare:41 | ||||
| chrX:47193616-47193861 | Rare:40; Clinvar:1 | ||||
| chrX:47218642-47218763 | Rare:63 | ||||
| chrX:47232909-47233036 | Rare:37 | ||||
| chrX:47233319-47233456 | Rare:22 | ||||
| chrX:47233716-47233830 | Common:1; Rare:16 | ||||
| chrX:47482517-47482726 | Common:5; Rare:48; Clinvar:4 | ||||
| chrX:47482916-47483039 | Rare:23 | ||||
| chrX:47483123-47483310 | Common:3; Rare:22 | ||||
| chrX:47560950-47561227 | Common:1; Rare:50 | ||||
| chrX:47561345-47561566 | Rare:37 |