| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3594963-3595139 | Rare:64 | ||||
| chr2:6866531-6866842 | Common:5; Rare:50 | ||||
| chr2:9423387-9423707 | Rare:99 | ||||
| chr2:9473661-9473841 | Rare:53 | ||||
| chr2:9555615-9555992 | Common:2; Rare:124 | ||||
| chr2:10689910-10690002 | Common:2; Rare:32 | ||||
| chr2:10812692-10812984 | Common:3; Rare:113 | ||||
| chr2:11746517-11746648 | Common:1; Rare:42; Clinvar:2 | ||||
| chr2:12716594-12717060 | Common:4; Rare:148 | ||||
| chr2:12718327-12718562 | Rare:71 | ||||
| chr2:15940332-15940592 | Rare:65 | ||||
| chr2:17540411-17540727 | Common:1; Rare:80 | ||||
| chr2:17753625-17754168 | Common:5; Rare:170; Clinvar (benign):1 | ||||
| chr2:18560673-18560801 | Rare:34 | ||||
| chr2:19901628-19902051 | Common:2; Rare:175 |