| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:124346430-124346603 | Common:1; Rare:15; Clinvar (benign):2 | ||||
| chrX:129906071-129906208 | Rare:33 | ||||
| chrX:130165683-130165920 | Rare:46; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chrX:130401884-130402024 | Common:2; Rare:41 | ||||
| chrX:132023160-132023311 | Rare:40 | ||||
| chrX:132219427-132219727 | Rare:30 | ||||
| chrX:132488917-132489133 | Rare:48 | ||||
| chrX:135032281-135032383 | Rare:28 | ||||
| chrX:135032648-135032917 | Rare:48 | ||||
| chrX:135052100-135052322 | Common:2; Rare:65 | ||||
| chrX:135344022-135344181 | Common:1; Rare:28 | ||||
| chrX:135344634-135344823 | Common:1; Rare:35 | ||||
| chrX:135973699-135973791 | Rare:32 | ||||
| chrX:139530528-139530857 | Common:2; Rare:51; Clinvar (benign):1 | ||||
| chrX:139933005-139933179 | Rare:33 |