| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70994822-70995053 | Common:4; Rare:70 | ||||
| chr2:71068523-71068678 | Rare:75 | ||||
| chr2:71130220-71130677 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071694-73071843 | Common:2; Rare:59 | ||||
| chr2:73234257-73234361 | Common:1; Rare:36 | ||||
| chr2:73385689-73386099 | Common:4; Rare:202; Clinvar:18; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73737228-73737553 | Common:3; Rare:106 | ||||
| chr2:73828804-73829024 | Common:1; Rare:51 | ||||
| chr2:73926795-73926934 | Common:1; Rare:85; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147866-74148100 | Common:1; Rare:65; Clinvar:2 | ||||
| chr2:74178812-74179026 | Common:2; Rare:62 | ||||
| chr2:74421579-74421759 | Rare:62 | ||||
| chr2:74440353-74440747 | Rare:96 | ||||
| chr2:74458113-74458514 | Common:1; Rare:124 | ||||
| chr2:74465346-74465439 | Rare:26; Clinvar:1 |