| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206765278-206765659 | Common:3; Rare:104; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165917-207166134 | Rare:43 | ||||
| chr2:207166182-207166387 | Common:3; Rare:90 | ||||
| chr2:207166833-207166972 | Common:1; Rare:63 | ||||
| chr2:207167177-207167490 | Common:2; Rare:65 | ||||
| chr2:207529525-207530126 | Common:3; Rare:155 | ||||
| chr2:207624559-207624686 | Rare:33 | ||||
| chr2:208254232-208254507 | Rare:71 | ||||
| chr2:208254991-208255253 | Common:2; Rare:67 | ||||
| chr2:208266053-208266396 | Common:8; Rare:115; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002495-210002659 | Common:4; Rare:55 | ||||
| chr2:210476675-210476872 | Rare:60 | ||||
| chr2:210477568-210477699 | Rare:41 | ||||
| chr2:213284186-213284483 | Rare:95 | ||||
| chr2:215311910-215312139 | Common:8; Rare:94 |