| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:8859-8934 | |||||
| chrM:8942-9547 | |||||
| chrM:9713-10013 | |||||
| chrM:10019-10139 | |||||
| chrM:10398-10531 | |||||
| chrM:10632-10988 | |||||
| chrM:10991-11476 | |||||
| chrM:13268-14222 | |||||
| chrM:14273-14773 | |||||
| chrX:1392036-1392367 | Common:6; Rare:146 | ||||
| chrX:11111139-11111307 | Common:1; Rare:30 | ||||
| chrX:12975074-12975118 | Rare:12 | ||||
| chrX:13734590-13734782 | Common:3; Rare:52; Clinvar (benign):1 | ||||
| chrX:14873047-14873219 | Common:1; Rare:37 | ||||
| chrX:30308281-30308398 | Rare:33 |