| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:55161090-55161332 | Rare:75 | ||||
| chrX:55452009-55452265 | Rare:38 | ||||
| chrX:56563360-56563725 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chrX:56729186-56729405 | Rare:29 | ||||
| chrX:56729442-56729574 | Common:1; Rare:15 | ||||
| chrX:56995354-56995632 | Common:1; Rare:55 | ||||
| chrX:56995635-56995822 | Rare:36 | ||||
| chrX:57121062-57121267 | Rare:34 | ||||
| chrX:57121396-57121670 | Common:1; Rare:63 | ||||
| chrX:63351257-63351560 | Common:1; Rare:70 | ||||
| chrX:63754696-63754759 | Rare:8 | ||||
| chrX:63755041-63755431 | Rare:78 | ||||
| chrX:63785130-63785304 | Rare:39; Clinvar (pathogenic):1 | ||||
| chrX:64205655-64205961 | Common:1; Rare:53 | ||||
| chrX:64976350-64976522 | Common:1; Rare:43 |