| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrX:135344003-135344215 | Common:1; Rare:34 | ||||
| chrX:135344626-135344830 | Common:1; Rare:40 | ||||
| chrX:135713293-135713674 | Common:7; Rare:42 | ||||
| chrX:135973698-135973802 | Rare:38 | ||||
| chrX:135973972-135974034 | Common:1; Rare:17 | ||||
| chrX:135985342-135985537 | Rare:61; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chrX:136147250-136147602 | Common:4; Rare:49 | ||||
| chrX:136250864-136250982 | Rare:29 | ||||
| chrX:136251292-136251723 | Rare:99 | ||||
| chrX:136497076-136497425 | Common:3; Rare:89 | ||||
| chrX:136880596-136880882 | Common:1; Rare:67 | ||||
| chrX:139204989-139205087 | Rare:12 | ||||
| chrX:139933005-139933162 | Rare:29 | ||||
| chrX:141002456-141002696 | Rare:5 | ||||
| chrX:141177070-141177325 | Common:1; Rare:33 |