| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104764057-104764193 | Common:2; Rare:30 | ||||
| chr9:105244321-105244652 | Common:1; Rare:121 | ||||
| chr9:105447959-105448153 | Common:2; Rare:72 | ||||
| chr9:105558044-105558184 | Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862431-106862773 | Common:4; Rare:88 | ||||
| chr9:106862951-106863186 | Rare:77 | ||||
| chr9:106863491-106863633 | Common:1; Rare:27 | ||||
| chr9:107282951-107283292 | Common:3; Rare:118 | ||||
| chr9:107283403-107283639 | Common:3; Rare:55 | ||||
| chr9:107488421-107488603 | Common:1; Rare:50 | ||||
| chr9:107489536-107489652 | Rare:17 | ||||
| chr9:107489767-107490073 | Common:4; Rare:135 | ||||
| chr9:108933913-108934504 | Common:9; Rare:232; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:109013303-109013552 | Common:2; Rare:82 | ||||
| chr9:109498246-109498419 | Rare:60 |