| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:16870899-16870981 | Common:1; Rare:27 | ||||
| chr9:19049326-19049457 | Rare:60 | ||||
| chr9:19102863-19103030 | Common:1; Rare:67 | ||||
| chr9:19127406-19127581 | Common:2; Rare:53 | ||||
| chr9:19379485-19379827 | Common:1; Rare:119 | ||||
| chr9:19380191-19380291 | Common:3; Rare:57 | ||||
| chr9:20684037-20684292 | Common:4; Rare:100 | ||||
| chr9:21031586-21031724 | Common:1; Rare:54 | ||||
| chr9:21802444-21802745 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:22009244-22009455 | Common:1; Rare:72 | ||||
| chr9:26892737-26892865 | Rare:67 | ||||
| chr9:26947132-26947325 | Rare:64 | ||||
| chr9:26956307-26956459 | Common:2; Rare:55 | ||||
| chr9:27529716-27529931 | Common:5; Rare:60 | ||||
| chr9:27573422-27573524 | Common:5; Rare:53 |