| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:134796258-134796421 | Common:1; Rare:11 | ||||
| chrX:134807089-134807281 | Rare:28 | ||||
| chrX:135032216-135032395 | Rare:44 | ||||
| chrX:135032503-135032753 | Rare:43 | ||||
| chrX:135344016-135344204 | Common:1; Rare:30 | ||||
| chrX:135344654-135344812 | Rare:30 | ||||
| chrX:135973687-135973850 | Rare:57 | ||||
| chrX:139933025-139933155 | Rare:25 | ||||
| chrX:141177037-141177289 | Common:1; Rare:36 | ||||
| chrX:149540799-149541016 | Common:3; Rare:40 | ||||
| chrX:149938440-149938632 | Common:1; Rare:50 | ||||
| chrX:150568305-150568660 | Common:1; Rare:78; Clinvar (benign):1 | ||||
| chrX:150693276-150693399 | Common:1; Rare:31 | ||||
| chrX:150898596-150898911 | Common:3; Rare:90 | ||||
| chrX:151397080-151397255 | Common:3; Rare:87 |