| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:136808910-136809215 | Common:1; Rare:70 | ||||
| chr9:136837076-136837371 | Common:1; Rare:90 | ||||
| chr9:136838770-136839360 | Common:5; Rare:254 | ||||
| chr9:136839365-136839881 | Common:1; Rare:203 | ||||
| chr9:136842169-136842486 | Common:1; Rare:94 | ||||
| chr9:136847853-136848203 | Rare:87 | ||||
| chr9:136863817-136864029 | Rare:51 | ||||
| chr9:136941445-136941534 | Rare:49 | ||||
| chr9:137198002-137198318 | Rare:64 | ||||
| chr9:137199307-137199556 | Rare:94; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr9:137217366-137217535 | Common:1; Rare:61 | ||||
| chr9:137223377-137223689 | Common:4; Rare:108 | ||||
| chr9:137296806-137296915 | Rare:17 | ||||
| chr9:137296929-137297253 | Common:1; Rare:53 | ||||
| chr9:137305112-137305213 | Rare:21 |