| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135973666-135973879 | Rare:71 | ||||
| chrX:135985315-135985723 | Rare:121; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chrX:136147250-136147619 | Common:4; Rare:51 | ||||
| chrX:136497066-136497439 | Common:3; Rare:97 | ||||
| chrX:136880656-136880882 | Common:1; Rare:55 | ||||
| chrX:137566452-137566614 | Rare:16 | ||||
| chrX:138711652-138711827 | Common:2; Rare:35 | ||||
| chrX:139203451-139203540 | Common:1; Rare:12 | ||||
| chrX:139933043-139933210 | Rare:31 | ||||
| chrX:141177030-141177325 | Common:1; Rare:45 | ||||
| chrX:143634935-143635178 | Rare:37 | ||||
| chrX:145817476-145818025 | Common:3; Rare:99 | ||||
| chrX:149505191-149505424 | Rare:70 | ||||
| chrX:149540799-149541074 | Common:4; Rare:53 | ||||
| chrX:149631731-149631868 | Common:1; Rare:32 |