| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:677358-677557 | Common:1; Rare:84 | ||||
| chr2:3377791-3377941 | Rare:40 | ||||
| chr2:3519516-3519605 | Common:1; Rare:29 | ||||
| chr2:3558263-3558471 | Common:5; Rare:89 | ||||
| chr2:3575107-3575349 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423410-9423707 | Rare:93 | ||||
| chr2:9555710-9555908 | Common:2; Rare:65 | ||||
| chr2:9843397-9843514 | Common:5; Rare:28 | ||||
| chr2:10689934-10689997 | Common:2; Rare:19 | ||||
| chr2:12716643-12717053 | Common:3; Rare:128 | ||||
| chr2:17540445-17540739 | Common:1; Rare:69 | ||||
| chr2:17753721-17753913 | Common:2; Rare:70 | ||||
| chr2:19901636-19902005 | Common:2; Rare:149 | ||||
| chr2:19990063-19990211 | Rare:37 | ||||
| chr2:20446876-20447074 | Common:2; Rare:70 |