| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:136880692-136880930 | Rare:106 | ||||
| chrX:139932941-139933270 | Rare:94 | ||||
| chrX:139933430-139933690 | Rare:57 | ||||
| chrX:141177026-141177373 | Common:3; Rare:102 | ||||
| chrX:147911704-147912187 | Common:5; Rare:228 | ||||
| chrX:149505224-149505420 | Rare:64 | ||||
| chrX:149540789-149541068 | Common:7; Rare:79 | ||||
| chrX:149631675-149631807 | Common:1; Rare:75 | ||||
| chrX:149938404-149938771 | Common:4; Rare:138 | ||||
| chrX:150363141-150363350 | Rare:30 | ||||
| chrX:150568320-150568653 | Common:2; Rare:135; Clinvar (benign):1 | ||||
| chrX:150693272-150693420 | Common:1; Rare:53 | ||||
| chrX:150898586-150898891 | Common:4; Rare:175 | ||||
| chrX:150983167-150983392 | Common:2; Rare:45 | ||||
| chrX:150983328-150983454 | Common:1; Rare:29 |