| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106862652-106862775 | Rare:25 | ||||
| chr9:106862916-106863180 | Rare:82 | ||||
| chr9:107488175-107488582 | Common:3; Rare:124 | ||||
| chr9:107489767-107490028 | Common:3; Rare:108 | ||||
| chr9:108933951-108933981 | Common:1; Rare:11; Clinvar:3 | ||||
| chr9:108934015-108934493 | Common:7; Rare:188; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498278-109498376 | Rare:34 | ||||
| chr9:110125320-110125576 | Rare:53 | ||||
| chr9:110127358-110127490 | Rare:21 | ||||
| chr9:110256418-110256671 | Common:2; Rare:93 | ||||
| chr9:110579359-110579642 | Common:2; Rare:88 | ||||
| chr9:110579784-110579817 | Common:1; Rare:9 | ||||
| chr9:110579837-110579962 | Common:1; Rare:40 | ||||
| chr9:110579973-110580040 | Rare:13 | ||||
| chr9:111038674-111038863 | Common:4; Rare:49 |