| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189441053-189441511 | Common:3; Rare:147 | ||||
| chr2:189580662-189580891 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:189783870-189784146 | Common:5; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189784281-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190343883-190344031 | Rare:28 | ||||
| chr2:190469296-190469569 | Common:2; Rare:45 | ||||
| chr2:190497305-190497549 | Rare:70 | ||||
| chr2:190534328-190534552 | Common:7; Rare:59 | ||||
| chr2:190534640-190534870 | Common:2; Rare:72 | ||||
| chr2:190648695-190648912 | Common:1; Rare:80 | ||||
| chr2:190880644-190880887 | Common:4; Rare:84 | ||||
| chr2:190880995-190881252 | Common:1; Rare:101 | ||||
| chr2:191014115-191014384 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191021011-191021130 | Common:1; Rare:19 | ||||
| chr2:191677823-191678201 | Common:4; Rare:107 |