| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3558269-3558695 | Common:6; Rare:151 | ||||
| chr2:3575098-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9423387-9423714 | Rare:102 | ||||
| chr2:9555703-9555992 | Common:2; Rare:97 | ||||
| chr2:9630364-9630844 | Common:6; Rare:200 | ||||
| chr2:9630950-9631180 | Common:2; Rare:80 | ||||
| chr2:9843250-9843502 | Common:6; Rare:70 | ||||
| chr2:10689910-10690015 | Common:2; Rare:37 | ||||
| chr2:10812697-10812974 | Common:3; Rare:110 | ||||
| chr2:11466127-11466198 | Common:1; Rare:21 | ||||
| chr2:11746517-11746655 | Common:1; Rare:43; Clinvar:2 | ||||
| chr2:12716651-12716975 | Common:2; Rare:101 | ||||
| chr2:15561290-15561380 | Rare:42 | ||||
| chr2:17518437-17518642 | Common:2; Rare:57 | ||||
| chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 |