| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:23907855-23907970 | Rare:24 | ||||
| chrX:24054898-24054987 | Rare:33 | ||||
| chrX:24465038-24465360 | Common:4; Rare:93 | ||||
| chrX:40580730-40581098 | Common:5; Rare:82; Clinvar (benign):4 | ||||
| chrX:41085254-41085892 | Common:3; Rare:161 | ||||
| chrX:41333597-41334288 | Common:8; Rare:167 | ||||
| chrX:41334332-41334640 | Common:2; Rare:110 | ||||
| chrX:41335014-41335116 | Rare:12 | ||||
| chrX:43656066-43656414 | Rare:62 | ||||
| chrX:44873028-44873199 | Rare:29 | ||||
| chrX:46545377-46545566 | Common:1; Rare:44; Clinvar (benign):1 | ||||
| chrX:47144609-47144843 | Common:1; Rare:42 | ||||
| chrX:47144885-47145375 | Rare:71 | ||||
| chrX:47218672-47218723 | Rare:23 | ||||
| chrX:47233333-47233456 | Rare:20 |