| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127796000-127796075 | Common:1; Rare:16 | ||||
| chr9:128112275-128112354 | Rare:8 | ||||
| chr9:128184204-128184481 | Common:1; Rare:46 | ||||
| chr9:128263032-128263241 | Rare:46 | ||||
| chr9:128272052-128272113 | Common:1; Rare:11 | ||||
| chr9:128582808-128583110 | Common:1; Rare:71; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:128684428-128684493 | Rare:9 | ||||
| chr9:128693986-128694210 | Common:1; Rare:56 | ||||
| chr9:128735458-128735755 | Common:2; Rare:61 | ||||
| chr9:128883005-128883211 | Common:1; Rare:48 | ||||
| chr9:128937152-128937207 | Rare:4 | ||||
| chr9:128945540-128945662 | Rare:18; Clinvar:1 | ||||
| chr9:128945775-128946090 | Rare:100; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
| chr9:128946791-128947026 | Rare:73; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:129006048-129006259 | Rare:71 |