| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132023135-132023341 | Rare:51 | ||||
| chrX:132218040-132218297 | Rare:30 | ||||
| chrX:132219422-132219649 | Rare:24 | ||||
| chrX:132489026-132489138 | Rare:17 | ||||
| chrX:134237102-134237237 | Rare:30 | ||||
| chrX:134373029-134373472 | Common:5; Rare:104 | ||||
| chrX:134797139-134797404 | Rare:44 | ||||
| chrX:134807110-134807281 | Rare:25 | ||||
| chrX:135022458-135022709 | Rare:56 | ||||
| chrX:135032179-135032483 | Rare:62 | ||||
| chrX:135052100-135052285 | Common:2; Rare:55 | ||||
| chrX:135344005-135344240 | Common:1; Rare:42 | ||||
| chrX:135344632-135344824 | Common:1; Rare:36 | ||||
| chrX:135973647-135973841 | Rare:64 | ||||
| chrX:135985305-135985510 | Rare:56; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 |