| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:130110679-130111080 | Rare:67 | ||||
| chrX:130165657-130165990 | Rare:124; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chrX:130268765-130268998 | Common:1; Rare:134 | ||||
| chrX:130339762-130339975 | Rare:61 | ||||
| chrX:130401871-130402038 | Common:4; Rare:101 | ||||
| chrX:130903143-130903549 | Common:2; Rare:126 | ||||
| chrX:131578692-131578802 | Common:1; Rare:22 | ||||
| chrX:132023073-132023352 | Rare:117 | ||||
| chrX:132217870-132218440 | Rare:119 | ||||
| chrX:132488870-132489090 | Rare:81 | ||||
| chrX:132489107-132489690 | Rare:129 | ||||
| chrX:132489891-132490156 | Common:1; Rare:75 | ||||
| chrX:134373095-134373432 | Common:10; Rare:169 | ||||
| chrX:134460016-134460315 | Common:6; Rare:150 | ||||
| chrX:134796450-134796840 | Rare:56 |