| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70978487-70978637 | Rare:39 | ||||
| chr2:70978893-70979191 | Common:4; Rare:84 | ||||
| chr2:71068526-71068710 | Rare:84 | ||||
| chr2:71129763-71129932 | Rare:35 | ||||
| chr2:71130215-71130677 | Common:6; Rare:131; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71453523-71453897 | Common:2; Rare:69 | ||||
| chr2:73070565-73070699 | Common:3; Rare:38 | ||||
| chr2:73071701-73071848 | Common:2; Rare:57 | ||||
| chr2:73214118-73214350 | Common:1; Rare:82 | ||||
| chr2:73225644-73225822 | Rare:55 | ||||
| chr2:73233173-73233464 | Common:2; Rare:80 | ||||
| chr2:73234102-73234381 | Common:2; Rare:75 | ||||
| chr2:73234567-73234592 | Rare:7 | ||||
| chr2:73385694-73386089 | Common:4; Rare:194; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73737275-73737473 | Common:2; Rare:58 |