| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107488434-107488615 | Common:1; Rare:50 | ||||
| chr9:107489767-107490037 | Common:3; Rare:113 | ||||
| chr9:108933951-108934003 | Common:1; Rare:23; Clinvar:4 | ||||
| chr9:108934012-108934478 | Common:7; Rare:182; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109119498-109119626 | Common:2; Rare:54 | ||||
| chr9:110048530-110048764 | Common:2; Rare:84 | ||||
| chr9:110125345-110125553 | Rare:42 | ||||
| chr9:110127370-110127479 | Rare:14 | ||||
| chr9:110579354-110579477 | Rare:45 | ||||
| chr9:110579746-110580103 | Common:2; Rare:84 | ||||
| chr9:111036264-111036310 | Rare:6 | ||||
| chr9:111038172-111038368 | Common:2; Rare:57 | ||||
| chr9:111038665-111038990 | Common:6; Rare:78 | ||||
| chr9:111661484-111661666 | Common:3; Rare:51 | ||||
| chr9:112379753-112380146 | Common:4; Rare:151 |