| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71276456-71276618 | Rare:56 | ||||
| chr2:72887274-72887459 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr2:73071298-73071485 | Common:1; Rare:64 | ||||
| chr2:73214187-73214326 | Common:1; Rare:61 | ||||
| chr2:73233183-73233468 | Common:1; Rare:79 | ||||
| chr2:73234182-73234364 | Common:2; Rare:54 | ||||
| chr2:73385593-73385878 | Common:2; Rare:107; Clinvar:8; Clinvar (benign):3 | ||||
| chr2:73386182-73386318 | Common:1; Rare:51; Clinvar (benign):3 | ||||
| chr2:73737304-73737663 | Common:3; Rare:115 | ||||
| chr2:73828798-73829037 | Common:1; Rare:54 | ||||
| chr2:73892704-73893055 | Common:3; Rare:67 | ||||
| chr2:74147866-74148115 | Common:1; Rare:67; Clinvar:2 | ||||
| chr2:74178758-74179065 | Common:3; Rare:87 | ||||
| chr2:74391792-74392142 | Common:2; Rare:164 | ||||
| chr2:74421567-74421753 | Rare:64 |