| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188292987-188293064 | Rare:10 | ||||
| chr2:189441053-189441511 | Common:3; Rare:147 | ||||
| chr2:189580724-189580994 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783879-189784078 | Common:3; Rare:60 | ||||
| chr2:189784271-189784543 | Common:4; Rare:101; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190180776-190181212 | Rare:113 | ||||
| chr2:190343856-190343949 | Rare:16 | ||||
| chr2:190534659-190534853 | Common:1; Rare:64 | ||||
| chr2:190648695-190648913 | Common:1; Rare:80 | ||||
| chr2:190880619-190880859 | Common:4; Rare:81 | ||||
| chr2:190881142-190881262 | Common:1; Rare:42 | ||||
| chr2:191014070-191014333 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191245231-191245515 | Common:3; Rare:91 | ||||
| chr2:191246162-191246326 | Common:1; Rare:45 | ||||
| chr2:191677854-191678218 | Common:4; Rare:103 |