| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:40755136-40755303 | Rare:45 | ||||
| chr9:40992064-40992368 | Common:7; Rare:24 | ||||
| chr9:41356873-41356891 | Common:1; Rare:1 | ||||
| chr9:41357801-41358052 | Rare:57 | ||||
| chr9:41358775-41358916 | Common:1; Rare:44 | ||||
| chr9:62802670-62802792 | |||||
| chr9:62838339-62838680 | Common:2; Rare:13 | ||||
| chr9:62898056-62898146 | Common:1; Rare:11 | ||||
| chr9:66268947-66269196 | Common:3; Rare:44 | ||||
| chr9:66269875-66270076 | Common:3; Rare:38 | ||||
| chr9:68640491-68640635 | Rare:24 | ||||
| chr9:70420092-70420309 | Common:3; Rare:59 | ||||
| chr9:92722792-92722939 | Rare:39; Clinvar (benign):2 | ||||
| chr9:92722998-92723185 | Common:1; Rare:26 | ||||
| chr9:92729322-92729495 | Rare:26 |