| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48958308-48958406 | Rare:30 | ||||
| chrX:49079831-49079963 | Rare:18 | ||||
| chrX:49123723-49123946 | Rare:47 | ||||
| chrX:53422620-53422911 | Common:1; Rare:79 | ||||
| chrX:53434342-53434533 | Common:1; Rare:44 | ||||
| chrX:53536210-53536513 | Common:3; Rare:52; Clinvar (benign):1 | ||||
| chrX:53683791-53683932 | Common:1; Rare:24 | ||||
| chrX:54440240-54440459 | Rare:43 | ||||
| chrX:54530047-54530325 | Common:2; Rare:39 | ||||
| chrX:55000204-55000416 | Rare:50 | ||||
| chrX:55161108-55161326 | Rare:67 | ||||
| chrX:56995494-56995613 | Common:1; Rare:23 | ||||
| chrX:57121461-57121574 | Common:1; Rare:23 | ||||
| chrX:63755086-63755431 | Rare:68 | ||||
| chrX:65034698-65034835 | Common:1; Rare:27 |