| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133256797-133257041 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr8:143281630-143281817 | Common:3; Rare:44 | ||||
| chr8:143816791-143816973 | Common:1; Rare:63 | ||||
| chr8:145002825-145003038 | Common:2; Rare:76 | ||||
| chr9:211060-211279 | Common:1; Rare:66 | ||||
| chr9:686451-686833 | Common:4; Rare:92 | ||||
| chr9:693594-693703 | Rare:31 | ||||
| chr9:1045473-1045695 | Common:5; Rare:62 | ||||
| chr9:4684797-4684927 | Rare:38 | ||||
| chr9:5629725-5630019 | Rare:71 | ||||
| chr9:13970563-13970693 | Rare:25 | ||||
| chr9:14316013-14316045 | Rare:7 | ||||
| chr9:16726857-16726933 | Rare:18 | ||||
| chr9:19378366-19378679 | Common:1; Rare:88 | ||||
| chr9:25677437-25677666 | Common:3; Rare:98 |