| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:72238969-72239141 | Rare:48 | ||||
| chrX:74614574-74614742 | Rare:30 | ||||
| chrX:75156277-75156369 | Common:2; Rare:24 | ||||
| chrX:75523009-75523212 | Common:1; Rare:42 | ||||
| chrX:75523244-75523546 | Common:3; Rare:42 | ||||
| chrX:76172928-76173138 | Rare:44 | ||||
| chrX:77786186-77786357 | Common:1; Rare:23 | ||||
| chrX:77895412-77895750 | Rare:93; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chrX:77910508-77910721 | Common:1; Rare:35 | ||||
| chrX:78103951-78104301 | Common:4; Rare:125 | ||||
| chrX:80809863-80810155 | Rare:36 | ||||
| chrX:81201911-81202192 | Rare:51 | ||||
| chrX:84502433-84502568 | Rare:17 | ||||
| chrX:85003738-85003909 | Common:2; Rare:32 | ||||
| chrX:85243860-85244157 | Common:2; Rare:61; Clinvar (benign):1 |