| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:4679437-4679669 | Rare:108 | ||||
| chr9:4792674-4793007 | Common:2; Rare:128 | ||||
| chr9:5437837-5437982 | Common:1; Rare:50 | ||||
| chr9:6015612-6015719 | Rare:47 | ||||
| chr9:6757865-6757970 | Common:2; Rare:32 | ||||
| chr9:15422641-15422876 | Common:1; Rare:98 | ||||
| chr9:17134857-17135062 | Rare:88 | ||||
| chr9:19380188-19380377 | Common:5; Rare:89 | ||||
| chr9:21802323-21802723 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:26892731-26892931 | Common:1; Rare:91 | ||||
| chr9:26947146-26947289 | Rare:51 | ||||
| chr9:33001568-33001746 | Common:3; Rare:87; Clinvar (benign):3 | ||||
| chr9:33025100-33025294 | Common:5; Rare:76 | ||||
| chr9:33076624-33076818 | Common:2; Rare:65 | ||||
| chr9:33290369-33290551 | Common:2; Rare:66 |