| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:129779817-129779975 | Rare:22 | ||||
| chrX:135344614-135344813 | Common:1; Rare:37 | ||||
| chrX:135973729-135973872 | Rare:45 | ||||
| chrX:136204783-136204921 | Rare:25 | ||||
| chrX:141177065-141177314 | Common:1; Rare:32 | ||||
| chrX:149540799-149541012 | Common:3; Rare:40 | ||||
| chrX:149938440-149938620 | Common:1; Rare:46 | ||||
| chrX:150898570-150898906 | Common:3; Rare:93 | ||||
| chrX:150983190-150983372 | Common:2; Rare:35 | ||||
| chrX:152830676-152831094 | Common:4; Rare:79 | ||||
| chrX:153794330-153794684 | Common:1; Rare:109; Clinvar (benign):2 | ||||
| chrX:153971169-153971274 | Rare:25 | ||||
| chrX:154398826-154398937 | Common:1; Rare:24 | ||||
| chrX:154428439-154428689 | Common:2; Rare:43 | ||||
| chrX:154486574-154486762 | Rare:30 |