| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207624559-207624686 | Rare:33 | ||||
| chr2:207625134-207625417 | Common:2; Rare:84 | ||||
| chr2:208025487-208025620 | Common:1; Rare:36 | ||||
| chr2:208253884-208254535 | Common:2; Rare:138 | ||||
| chr2:208254917-208255238 | Common:2; Rare:83 | ||||
| chr2:208266121-208266355 | Common:6; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002488-210002688 | Common:5; Rare:75 | ||||
| chr2:210170632-210170898 | Common:1; Rare:99 | ||||
| chr2:210477572-210477695 | Rare:41 | ||||
| chr2:213284161-213284497 | Rare:102 | ||||
| chr2:215311873-215312144 | Common:8; Rare:104 | ||||
| chr2:215435998-215436274 | Common:2; Rare:86 | ||||
| chr2:216081737-216081925 | Common:1; Rare:66 | ||||
| chr2:216412694-216412786 | Rare:11 | ||||
| chr2:216498711-216498894 | Common:7; Rare:77 |