| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:47482556-47482670 | Common:5; Rare:25; Clinvar:2 | ||||
| chrX:47483138-47483397 | Common:3; Rare:32 | ||||
| chrX:47658611-47658824 | Rare:36 | ||||
| chrX:47836640-47836961 | Common:1; Rare:66 | ||||
| chrX:48468300-48468384 | Rare:13 | ||||
| chrX:48476091-48476253 | Rare:32 | ||||
| chrX:48508861-48509027 | Rare:32 | ||||
| chrX:48521791-48521905 | Rare:23 | ||||
| chrX:48574197-48574573 | Common:2; Rare:101 | ||||
| chrX:48574875-48575282 | Common:3; Rare:95 | ||||
| chrX:48696584-48696790 | Rare:48 | ||||
| chrX:48911607-48911715 | Rare:27; Clinvar (benign):4 | ||||
| chrX:48957880-48957912 | Rare:9 | ||||
| chrX:49002193-49002295 | Rare:34 | ||||
| chrX:49043497-49043821 | Rare:56 |