| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:103356122-103356603 | Common:4; Rare:65 | ||||
| chrX:103356618-103356904 | Rare:45 | ||||
| chrX:103376406-103376613 | Common:1; Rare:33 | ||||
| chrX:103585455-103585682 | Common:3; Rare:46 | ||||
| chrX:103586429-103586885 | Rare:97 | ||||
| chrX:103607663-103608067 | Common:1; Rare:65 | ||||
| chrX:103628877-103629007 | Rare:16 | ||||
| chrX:103629445-103629545 | Rare:26 | ||||
| chrX:103686622-103686895 | Common:1; Rare:43 | ||||
| chrX:103688004-103688234 | Common:1; Rare:30 | ||||
| chrX:103919027-103919155 | Common:4; Rare:26 | ||||
| chrX:104156891-104157069 | Common:1; Rare:29 | ||||
| chrX:104166625-104166776 | Rare:24 | ||||
| chrX:107118571-107118889 | Common:3; Rare:58 | ||||
| chrX:107628304-107628531 | Common:1; Rare:28; Clinvar (benign):1 |