| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55231654-55232073 | Common:4; Rare:96 | ||||
| chr2:55232242-55232806 | Common:5; Rare:170 | ||||
| chr2:55268682-55268975 | Common:1; Rare:65 | ||||
| chr2:55419792-55419997 | Common:4; Rare:87 | ||||
| chr2:55519407-55519876 | Common:2; Rare:156 | ||||
| chr2:55923714-55923894 | Common:3; Rare:61; Clinvar (benign):7 | ||||
| chr2:58046598-58046885 | Common:2; Rare:90 | ||||
| chr2:58241316-58241431 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:61017171-61017352 | Common:4; Rare:48 | ||||
| chr2:61017408-61017767 | Common:1; Rare:111; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:61066569-61066861 | Common:1; Rare:78 | ||||
| chr2:61144837-61145196 | Common:3; Rare:112 | ||||
| chr2:61177131-61177536 | Common:6; Rare:159 | ||||
| chr2:61184505-61184787 | Common:1; Rare:73 | ||||
| chr2:61185490-61186174 | Common:4; Rare:236 |