| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136847832-136848178 | Rare:78 | ||||
| chr9:136854725-136854812 | Rare:44 | ||||
| chr9:136863433-136863498 | Rare:15 | ||||
| chr9:136863817-136863995 | Rare:43 | ||||
| chr9:136941650-136941735 | Rare:41 | ||||
| chr9:137050965-137051244 | Common:4; Rare:109 | ||||
| chr9:137129698-137129822 | Common:2; Rare:38 | ||||
| chr9:137198002-137198317 | Rare:64 | ||||
| chr9:137217388-137217508 | Common:1; Rare:35 | ||||
| chr9:137254166-137254360 | Rare:33 | ||||
| chr9:137296779-137296908 | Common:2; Rare:21 | ||||
| chr9:137307649-137307794 | Common:2; Rare:44 | ||||
| chr9:137309654-137309846 | Rare:50 | ||||
| chr9:137433486-137433864 | Common:2; Rare:105 | ||||
| chr9:137776481-137776722 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 |