| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210170610-210171010 | Common:8; Rare:615 | ||||
| chr2:210171210-210171663 | Common:22; Rare:646 | ||||
| chr2:210476590-210476990 | Common:6; Rare:301 | ||||
| chr2:210477400-210477750 | Common:2; Rare:318; Clinvar (benign):2 | ||||
| chr2:213151570-213152050 | Common:5; Rare:650 | ||||
| chr2:213284142-213284878 | Rare:629 | ||||
| chr2:214809053-214809457 | Common:9; Rare:160; Clinvar:9; Clinvar (benign):9 | ||||
| chr2:214809501-214810280 | Common:55; Rare:1076; Clinvar:19; Clinvar (benign):18 | ||||
| chr2:215311778-215312172 | Common:62; Rare:858 | ||||
| chr2:215312318-215312718 | Common:4; Rare:235 | ||||
| chr2:215420413-215420823 | Common:4; Rare:214 | ||||
| chr2:215435993-215436411 | Common:13; Rare:547 | ||||
| chr2:216012890-216013430 | Common:3; Rare:180 | ||||
| chr2:216013443-216013850 | Common:4; Rare:152 | ||||
| chr2:216081667-216082067 | Common:6; Rare:358 |