| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136400133-136400303 | Common:2; Rare:61 | ||||
| chr9:136839545-136839693 | Common:1; Rare:44 | ||||
| chrM:1530-1608 | |||||
| chrM:15884-15888 | |||||
| chrM:15950-15966 | |||||
| chrX:15675080-15675151 | Rare:21 | ||||
| chrX:15675606-15675735 | Common:1; Rare:24 | ||||
| chrX:48901991-48902234 | Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
| chrX:74292581-74292743 | Rare:24 | ||||
| chrX:103330777-103331006 | Common:2; Rare:36 | ||||
| chrX:131830568-131830828 | Rare:40 | ||||
| chrX:154361327-154361781 | Common:1; Rare:90; Clinvar:10; Clinvar (benign):15 | ||||
| chrX:154366306-154366633 | Common:1; Rare:97; Clinvar:7; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chrX:154367639-154368083 | Common:2; Rare:69; Clinvar:6; Clinvar (benign):9 | ||||
| chrX:154368886-154369150 | Rare:47 |