| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132488870-132489011 | Rare:39 | ||||
| chrX:133985273-133985650 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):7 | ||||
| chrX:134797139-134797404 | Rare:44 | ||||
| chrX:134807087-134807284 | Rare:29 | ||||
| chrX:135052090-135052458 | Common:3; Rare:95 | ||||
| chrX:135343984-135344221 | Common:1; Rare:37 | ||||
| chrX:135344592-135344823 | Common:2; Rare:42 | ||||
| chrX:135973695-135973789 | Rare:31 | ||||
| chrX:139933001-139933222 | Rare:46 | ||||
| chrX:141177070-141177304 | Common:1; Rare:29 | ||||
| chrX:149540874-149541082 | Common:3; Rare:38 | ||||
| chrX:149938404-149938667 | Common:2; Rare:65 | ||||
| chrX:150898586-150898911 | Common:3; Rare:92 | ||||
| chrX:151397054-151397289 | Common:4; Rare:119 | ||||
| chrX:151974673-151974981 | Common:1; Rare:84 |