| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143934032-143934328 | Common:2; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:145002816-145003045 | Common:2; Rare:85 | ||||
| chr9:684204-684292 | Common:2; Rare:25 | ||||
| chr9:686444-686889 | Common:5; Rare:103 | ||||
| chr9:693504-693742 | Rare:61 | ||||
| chr9:694889-695080 | Rare:45 | ||||
| chr9:696170-696434 | Common:1; Rare:72 | ||||
| chr9:2015864-2016090 | Common:1; Rare:74 | ||||
| chr9:5768905-5769010 | Rare:35 | ||||
| chr9:6681230-6681483 | Common:6; Rare:106 | ||||
| chr9:13278012-13278096 | Common:1; Rare:21 | ||||
| chr9:13970501-13970693 | Rare:40 | ||||
| chr9:15486854-15486987 | Common:2; Rare:47 | ||||
| chr9:16337449-16337662 | Rare:47 | ||||
| chr9:16726834-16726955 | Common:1; Rare:29 |