| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19380165-19380340 | Common:5; Rare:90 | ||||
| chr9:19408782-19409021 | Common:3; Rare:92 | ||||
| chr9:20658173-20658349 | Common:4; Rare:64 | ||||
| chr9:20684037-20684283 | Common:4; Rare:95 | ||||
| chr9:21031595-21031735 | Common:1; Rare:52 | ||||
| chr9:21335338-21335521 | Common:3; Rare:65 | ||||
| chr9:21802323-21802733 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:22009181-22009478 | Common:1; Rare:101 | ||||
| chr9:26892431-26892480 | Rare:24 | ||||
| chr9:26892735-26892895 | Common:1; Rare:79 | ||||
| chr9:26947078-26947281 | Common:1; Rare:80 | ||||
| chr9:26947409-26947562 | Common:1; Rare:50 | ||||
| chr9:26956248-26956464 | Common:2; Rare:80 | ||||
| chr9:27529716-27529799 | Common:2; Rare:24 | ||||
| chr9:27573391-27573564 | Common:6; Rare:98 |