| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136483746-136483880 | Rare:41 | ||||
| chr9:136662787-136662966 | Common:1; Rare:49 | ||||
| chr9:136849632-136849803 | Common:1; Rare:57 | ||||
| chr9:136886250-136886541 | Common:2; Rare:85 | ||||
| chr9:136979946-136980283 | Rare:137 | ||||
| chr9:136992179-136992471 | Rare:88 | ||||
| chr9:137086661-137087214 | Common:3; Rare:224; Clinvar:7; Clinvar (benign):3 | ||||
| chr9:137188528-137188738 | Common:2; Rare:103 | ||||
| chr9:137205646-137205741 | Rare:39 | ||||
| chr9:137423121-137423523 | Common:2; Rare:126 | ||||
| chr9:137550345-137550496 | Rare:21 | ||||
| chr9:137551647-137551978 | Common:28; Rare:145 | ||||
| chr9:137578828-137579056 | Common:2; Rare:72 | ||||
| chr9:137612627-137612970 | Common:2; Rare:103 | ||||
| chr9:137618747-137619046 | Common:1; Rare:133 |