| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:49079789-49080001 | Rare:53 | ||||
| chrX:49101071-49101411 | Common:4; Rare:129 | ||||
| chrX:49123716-49124067 | Rare:94 | ||||
| chrX:49163670-49164100 | Common:4; Rare:174 | ||||
| chrX:49164080-49164430 | Common:4; Rare:89 | ||||
| chrX:49186285-49186505 | Common:2; Rare:67 | ||||
| chrX:49200148-49200358 | Rare:109; Clinvar:2 | ||||
| chrX:49235548-49235948 | Common:7; Rare:103 | ||||
| chrX:49269540-49270080 | Rare:193 | ||||
| chrX:49879130-49879770 | Common:2; Rare:197 | ||||
| chrX:49922324-49922735 | Common:2; Rare:166 | ||||
| chrX:50067251-50067631 | Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:51893259-51893753 | Common:4; Rare:178 | ||||
| chrX:52995201-52996000 | Common:12; Rare:198 | ||||
| chrX:53082543-53083090 | Common:1; Rare:212; Clinvar (benign):1 |