| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101398505-101398893 | Common:1; Rare:142 | ||||
| chr9:101487043-101487119 | Rare:29 | ||||
| chr9:101487122-101487185 | Common:1; Rare:13 | ||||
| chr9:101487193-101487248 | Common:1; Rare:11 | ||||
| chr9:101533724-101533899 | Rare:53 | ||||
| chr9:104093985-104094317 | Common:3; Rare:78 | ||||
| chr9:104094431-104094603 | Common:2; Rare:46 | ||||
| chr9:104747609-104747836 | Common:1; Rare:79 | ||||
| chr9:106862978-106863180 | Rare:69 | ||||
| chr9:107489767-107490034 | Common:3; Rare:111 | ||||
| chr9:108933931-108933985 | Common:2; Rare:18; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:108934042-108934493 | Common:7; Rare:178; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013452-109013774 | Common:2; Rare:113 | ||||
| chr9:109498238-109498464 | Rare:70 | ||||
| chr9:110256410-110256725 | Common:5; Rare:109 |