| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:107282962-107283292 | Common:2; Rare:113 | ||||
| chr9:107488417-107488577 | Common:1; Rare:47 | ||||
| chr9:107489767-107490022 | Common:3; Rare:105 | ||||
| chr9:108933951-108933985 | Common:1; Rare:12; Clinvar:3 | ||||
| chr9:108934065-108934493 | Common:7; Rare:170; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109013438-109013784 | Common:2; Rare:121 | ||||
| chr9:109498248-109498433 | Rare:62 | ||||
| chr9:110125345-110125578 | Rare:45 | ||||
| chr9:110127196-110127474 | Rare:46 | ||||
| chr9:111038190-111038349 | Common:2; Rare:48 | ||||
| chr9:111599389-111599754 | Common:2; Rare:85 | ||||
| chr9:112379800-112380218 | Common:3; Rare:159 | ||||
| chr9:113056674-113056829 | Rare:57 | ||||
| chr9:113221262-113221594 | Rare:106 | ||||
| chr9:113275354-113275728 | Common:5; Rare:121; Clinvar (pathogenic):1 |