| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:189784250-189784787 | Common:9; Rare:170; Clinvar:8; Clinvar (benign):4 | ||||
| chr2:190180201-190180540 | Common:3; Rare:74 | ||||
| chr2:190180734-190180908 | Rare:51 | ||||
| chr2:190319179-190319334 | Rare:31 | ||||
| chr2:190319685-190320116 | Common:5; Rare:138; Clinvar (benign):6 | ||||
| chr2:190343571-190343745 | Common:2; Rare:45 | ||||
| chr2:190359951-190360082 | Common:1; Rare:24 | ||||
| chr2:190408108-190408292 | Rare:44 | ||||
| chr2:190408641-190408888 | Common:3; Rare:54 | ||||
| chr2:190468999-190469055 | Common:1; Rare:8 | ||||
| chr2:190534274-190534944 | Common:11; Rare:207 | ||||
| chr2:190648656-190648862 | Common:1; Rare:76 | ||||
| chr2:190649388-190649619 | Common:1; Rare:68 | ||||
| chr2:190880333-190880406 | Common:1; Rare:20 | ||||
| chr2:190880481-190881039 | Common:5; Rare:197 |