| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chrM:3168-3244 | |||||
| chrM:3577-4058 | |||||
| chrM:4327-4332 | |||||
| chrM:7398-8118 | |||||
| chrM:8274-8409 | |||||
| chrM:9060-9438 | |||||
| chrM:10468-10725 | |||||
| chrM:12474-12818 | |||||
| chrM:14427-14469 | |||||
| chrM:14480-14858 | |||||
| chrM:14946-15261 | |||||
| chrX:2929309-2929513 | Common:2; Rare:57 | ||||
| chrX:7927704-7927779 | Rare:15 | ||||
| chrX:11111141-11111356 | Common:3; Rare:45 | ||||
| chrX:13734577-13734854 | Common:3; Rare:83; Clinvar (benign):1 |