| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:137086587-137087146 | Common:2; Rare:230; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:137102813-137103077 | Common:7; Rare:39 | ||||
| chr9:137107460-137107550 | Common:1; Rare:33; Clinvar (benign):1 | ||||
| chr9:137114695-137114984 | Common:2; Rare:116 | ||||
| chr9:137171989-137172177 | Rare:47 | ||||
| chr9:137183145-137183446 | Common:2; Rare:85 | ||||
| chr9:137188532-137188744 | Common:2; Rare:105 | ||||
| chr9:137188862-137189029 | Common:2; Rare:51 | ||||
| chr9:137205389-137205763 | Common:1; Rare:140 | ||||
| chr9:137240896-137241829 | Common:7; Rare:405 | ||||
| chr9:137247727-137247876 | Common:1; Rare:48 | ||||
| chr9:137251126-137251351 | Rare:69 | ||||
| chr9:137255113-137255463 | Common:7; Rare:126 | ||||
| chr9:137423211-137423523 | Common:2; Rare:94 | ||||
| chr9:137453986-137454207 | Common:1; Rare:34 |