| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137618767-137619031 | Common:1; Rare:120 | ||||
| chr9:137815845-137816063 | Common:1; Rare:62; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chrM:1957-2890 | |||||
| chrM:2937-3834 | |||||
| chrM:3871-4147 | |||||
| chrM:4310-4449 | |||||
| chrM:4455-4729 | |||||
| chrM:4814-5082 | |||||
| chrM:5146-5579 | |||||
| chrM:5582-6023 | |||||
| chrM:6177-6731 | |||||
| chrM:7103-7704 | |||||
| chrM:7766-7953 | |||||
| chrM:8019-8758 | |||||
| chrM:8899-9165 |