| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392637-177393070 | Common:3; Rare:147; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:178478545-178478721 | Common:1; Rare:56 | ||||
| chr2:186486110-186486348 | Common:3; Rare:77 | ||||
| chr2:188292692-188292972 | Common:1; Rare:65 | ||||
| chr2:188293005-188293064 | Rare:7 | ||||
| chr2:188293736-188293852 | Rare:19 | ||||
| chr2:189179506-189179526 | Rare:4 | ||||
| chr2:189441086-189441519 | Common:2; Rare:135 | ||||
| chr2:189783965-189784078 | Common:2; Rare:38 | ||||
| chr2:189784276-189784537 | Common:4; Rare:93; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190880590-190880859 | Common:4; Rare:94 | ||||
| chr2:191014139-191014319 | Common:1; Rare:54; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677856-191678173 | Common:4; Rare:91 | ||||
| chr2:192194907-192195054 | Rare:28 | ||||
| chr2:197434989-197435176 | Rare:63 |