| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15510191-15510458 | Common:1; Rare:119 | ||||
| chr9:19049337-19049928 | Common:4; Rare:183 | ||||
| chr9:19376309-19376538 | Common:2; Rare:80 | ||||
| chr9:19380184-19380381 | Common:5; Rare:95 | ||||
| chr9:20622289-20622545 | Rare:97 | ||||
| chr9:21335347-21335483 | Common:3; Rare:53 | ||||
| chr9:21994301-21994791 | Common:2; Rare:141; Clinvar:4; Clinvar (benign):6 | ||||
| chr9:21994923-21995100 | Common:1; Rare:28 | ||||
| chr9:26892332-26892440 | Rare:49 | ||||
| chr9:26892706-26892876 | Rare:83 | ||||
| chr9:26947107-26947299 | Common:1; Rare:69 | ||||
| chr9:32552557-32552904 | Common:2; Rare:86; Clinvar:2 | ||||
| chr9:33025071-33025378 | Common:7; Rare:126 | ||||
| chr9:33076610-33076841 | Common:2; Rare:81 | ||||
| chr9:33166779-33166948 | Rare:59; Clinvar:2 |