| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:130165660-130165927 | Rare:52; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401884-130402037 | Common:2; Rare:45 | ||||
| chrX:132218077-132218280 | Rare:23 | ||||
| chrX:134796255-134796439 | Common:1; Rare:16 | ||||
| chrX:134990806-134991026 | Rare:29 | ||||
| chrX:134991433-134991733 | Common:2; Rare:30 | ||||
| chrX:135022438-135022732 | Rare:68 | ||||
| chrX:135344005-135344195 | Common:1; Rare:30 | ||||
| chrX:135344626-135344821 | Common:1; Rare:36 | ||||
| chrX:136497365-136497642 | Common:1; Rare:59 | ||||
| chrX:141177022-141177327 | Common:1; Rare:48 | ||||
| chrX:149540811-149541077 | Common:4; Rare:50 | ||||
| chrX:149938434-149938616 | Common:1; Rare:46 | ||||
| chrX:150363142-150363322 | Rare:14 | ||||
| chrX:150983064-150983339 | Common:2; Rare:51 |