| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:30447111-30447349 | Common:5; Rare:95 | ||||
| chr2:32010214-32010520 | Rare:86 | ||||
| chr2:32010528-32010733 | Rare:50 | ||||
| chr2:32010740-32011269 | Common:2; Rare:150 | ||||
| chr2:32039684-32040072 | Common:3; Rare:104 | ||||
| chr2:32040094-32040144 | Rare:10 | ||||
| chr2:32063340-32063762 | Common:1; Rare:146; Clinvar:1 | ||||
| chr2:32063847-32064047 | Common:1; Rare:100; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:32165603-32166034 | Common:3; Rare:164 | ||||
| chr2:32264766-32264823 | Common:1; Rare:10 | ||||
| chr2:32277713-32277990 | Common:1; Rare:64 | ||||
| chr2:32278082-32278263 | Rare:61 | ||||
| chr2:32356594-32357272 | Common:7; Rare:237 | ||||
| chr2:32627871-32628198 | Rare:95 | ||||
| chr2:33476147-33476235 | Common:1; Rare:14 |