| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:989-1347 | |||||
| chrM:1486-1604 | |||||
| chrM:11363-11481 | |||||
| chrM:12995-13067 | |||||
| chrM:13507-13804 | |||||
| chrM:15883-15967 | |||||
| chrX:19683070-19683265 | Rare:27 | ||||
| chrX:47129553-47129642 | Common:1; Rare:7 | ||||
| chrX:73944170-73944375 | Common:1; Rare:59 | ||||
| chrX:74420714-74420866 | Rare:37 | ||||
| chrX:154362303-154362532 | Common:1; Rare:69; Clinvar:7; Clinvar (benign):6 | ||||
| chrX:154366374-154366588 | Rare:68; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chrX:154367655-154367961 | Common:2; Rare:53; Clinvar:3; Clinvar (benign):6 | ||||
| chrY:12662161-12662403 | Rare:1 |