| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:62802005-62802068 | Not yet | Rare:1 | 115 | ||
| chr9:62802628-62802781 | Not yet | 186 | |||
| chr9:73158597-73158734 | Not yet | Rare:47 | 283 | ||
| chr9:87728100-87728809 | Not yet | Common:2; Rare:191 | 538 | ||
| chr9:107734663-107734863 | Not yet | Common:3; Rare:39 | 251 | ||
| chr9:125238665-125238965 | Not yet | Common:1; Rare:81 | 323 | ||
| chr9:129698654-129698762 | Not yet | Rare:21 | 203 | ||
| chr9:136438931-136439099 | Not yet | Rare:63; Clinvar (pathogenic):1 | 191 | ||
| chr9:136728159-136728331 | Not yet | Common:2; Rare:76 | 212 | ||
| chr9:137223387-137223681 | Not yet | Common:3; Rare:103 | 340 | ||
| chrM:260-839 | Not yet | 493 | |||
| chrM:1667-1792 | Not yet | 191 | |||
| chrM:1806-2655 | Not yet | 535 | |||
| chrM:6519-6733 | Not yet | 247 | |||
| chrM:6891-6981 | Not yet | 129 |