| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101533664-101533914 | Common:2; Rare:79 | ||||
| chr9:104093985-104094327 | Common:3; Rare:80 | ||||
| chr9:104747631-104747799 | Common:1; Rare:53 | ||||
| chr9:105447959-105448176 | Common:2; Rare:80 | ||||
| chr9:105694381-105694624 | Common:4; Rare:102 | ||||
| chr9:106862141-106862665 | Common:4; Rare:141 | ||||
| chr9:106862699-106862804 | Rare:23 | ||||
| chr9:106862854-106863195 | Rare:99 | ||||
| chr9:106863490-106863900 | Common:1; Rare:100 | ||||
| chr9:107282940-107283289 | Common:3; Rare:123 | ||||
| chr9:108933931-108934551 | Common:10; Rare:244; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:109166923-109167304 | Common:1; Rare:113; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr9:109498233-109498375 | Rare:46 | ||||
| chr9:111525014-111525240 | Common:5; Rare:73 | ||||
| chr9:111599787-111599892 | Common:1; Rare:37 |