| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178689295-178689598 | Common:1; Rare:73; Clinvar:5; Clinvar (benign):3 | ||||
| chr2:178828126-178828332 | Common:4; Rare:46 | ||||
| chr2:179561809-179561972 | Common:2; Rare:28 | ||||
| chr2:187473815-187473945 | Common:3; Rare:29 | ||||
| chr2:187550917-187551088 | Common:2; Rare:24 | ||||
| chr2:187672667-187672739 | Common:4; Rare:13 | ||||
| chr2:187673769-187673861 | Common:1; Rare:24 | ||||
| chr2:187673893-187674013 | Common:3; Rare:38 | ||||
| chr2:190499961-190500052 | Common:2; Rare:26 | ||||
| chr2:190881980-190882065 | Common:2; Rare:20 | ||||
| chr2:190901813-190902019 | Rare:49 | ||||
| chr2:190925580-190925588 | Rare:2 | ||||
| chr2:190948848-190949003 | Rare:32 | ||||
| chr2:190950643-190950744 | Common:1; Rare:21 | ||||
| chr2:190961703-190961790 | Common:1; Rare:13 |