| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107488401-107488582 | Common:1; Rare:51 | ||||
| chr9:107488588-107488630 | Rare:9 | ||||
| chr9:107488927-107489171 | Rare:94 | ||||
| chr9:107489767-107490078 | Common:4; Rare:137 | ||||
| chr9:107490216-107490341 | Rare:38 | ||||
| chr9:108934042-108934493 | Common:7; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013426-109013661 | Common:2; Rare:84 | ||||
| chr9:109119464-109119560 | Common:2; Rare:42 | ||||
| chr9:109498259-109498423 | Rare:56 | ||||
| chr9:110048489-110048800 | Common:3; Rare:105; Clinvar (benign):1 | ||||
| chr9:110125315-110125332 | Rare:5 | ||||
| chr9:110125345-110125576 | Rare:45 | ||||
| chr9:110127351-110127467 | Rare:15 | ||||
| chr9:110256410-110256729 | Common:5; Rare:110 | ||||
| chr9:110256857-110257056 | Rare:41 |