| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15469938-15470224 | Rare:90 | ||||
| chr9:32550845-32551103 | Common:1; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:40991963-40992356 | Common:7; Rare:32 | ||||
| chr9:41274005-41274213 | Common:2; Rare:25 | ||||
| chr9:62801302-62801480 | Common:1; Rare:2 | ||||
| chr9:62838354-62838547 | Common:2; Rare:9 | ||||
| chr9:62897695-62897765 | Rare:19 | ||||
| chr9:70413429-70413637 | Rare:63 | ||||
| chr9:83219195-83219345 | Common:2; Rare:37 | ||||
| chr9:89180391-89180569 | Common:3; Rare:26 | ||||
| chr9:113012164-113012277 | Rare:22 | ||||
| chr9:124000279-124000415 | Rare:32 | ||||
| chr9:124658258-124658441 | Rare:35 | ||||
| chrM:397-566 | |||||
| chrM:572-1386 |