| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:77822975-77823041 | Common:1; Rare:13 | ||||
| chr9:87713522-87713625 | Common:2; Rare:9 | ||||
| chr9:88534132-88534257 | Common:1; Rare:34 | ||||
| chr9:94554936-94555102 | Common:4; Rare:37 | ||||
| chrM:294-846 | |||||
| chrM:848-1007 | |||||
| chrM:15937-15955 | |||||
| chrX:2609154-2609421 | Rare:85 | ||||
| chrX:29660086-29660212 | Common:4; Rare:17 | ||||
| chrX:45771230-45771487 | Rare:30 | ||||
| chrX:73944167-73944370 | Common:1; Rare:58 | ||||
| chrX:74292530-74292743 | Rare:37 | ||||
| chrX:96465857-96465969 | Rare:15 | ||||
| chrX:154366132-154366369 | Common:3; Rare:71; Clinvar:8; Clinvar (benign):9 | ||||
| chrX:154368887-154369143 | Rare:47 |