| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:132955699-132955986 | Rare:41 | ||||
| chrX:132957248-132957444 | Common:1; Rare:42 | ||||
| chrX:135032928-135033063 | Rare:17 | ||||
| chrX:136909295-136909465 | Rare:46 | ||||
| chrX:153245352-153245667 | Common:1; Rare:50 | ||||
| chrX:153866855-153867121 | Common:2; Rare:40; Clinvar (benign):2 | ||||
| chrX:153925465-153925714 | Rare:47 | ||||
| chrY:12662198-12662455 | Rare:3 |