| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:20267064-20267270 | Common:1; Rare:37 | ||||
| chrX:21374126-21374418 | Common:1; Rare:67 | ||||
| chrX:23667367-23667591 | Common:2; Rare:70 | ||||
| chrX:23782948-23783314 | Common:5; Rare:77 | ||||
| chrX:23907880-23908086 | Rare:44 | ||||
| chrX:28587059-28587135 | Rare:4 | ||||
| chrX:37847512-37847677 | Common:1; Rare:42 | ||||
| chrX:38327483-38327682 | Rare:52 | ||||
| chrX:40735290-40735647 | Rare:93 | ||||
| chrX:41333839-41334193 | Common:4; Rare:90 | ||||
| chrX:43656086-43656352 | Rare:51 | ||||
| chrX:44542805-44543056 | Common:1; Rare:54 | ||||
| chrX:46545377-46545524 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chrX:47144668-47145291 | Common:1; Rare:90 | ||||
| chrX:47482568-47482701 | Common:5; Rare:32; Clinvar:3 |