| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:48469336-48469594 | Rare:35 | ||||
| chrX:48475857-48476339 | Rare:157 | ||||
| chrX:48508260-48508671 | Rare:78 | ||||
| chrX:48508784-48509058 | Common:2; Rare:93 | ||||
| chrX:48521522-48522193 | Common:8; Rare:217; Clinvar (benign):2 | ||||
| chrX:48539358-48539778 | Common:3; Rare:127 | ||||
| chrX:48574300-48574522 | Common:2; Rare:131 | ||||
| chrX:48574861-48575217 | Common:3; Rare:120 | ||||
| chrX:48597372-48597559 | Rare:57 | ||||
| chrX:48597666-48597873 | Common:2; Rare:43 | ||||
| chrX:48676324-48676660 | Common:2; Rare:137 | ||||
| chrX:48696536-48696799 | Common:1; Rare:106 | ||||
| chrX:48696810-48697250 | Rare:182 | ||||
| chrX:48801316-48801428 | Common:1; Rare:15 | ||||
| chrX:48801609-48801824 | Common:1; Rare:41 |