| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171752009-171752283 | Common:2; Rare:57 | ||||
| chr2:171752621-171752663 | Rare:7 | ||||
| chr2:171762519-171762787 | Common:1; Rare:58 | ||||
| chr2:171765591-171765892 | Rare:48 | ||||
| chr2:171770377-171770575 | Rare:45 | ||||
| chr2:171772167-171772387 | Common:1; Rare:50 | ||||
| chr2:171772510-171772798 | Common:5; Rare:71 | ||||
| chr2:171775569-171775929 | Common:2; Rare:51 | ||||
| chr2:171776409-171776678 | Common:3; Rare:37 | ||||
| chr2:171781729-171781809 | Rare:14 | ||||
| chr2:171782157-171782354 | Common:1; Rare:37 | ||||
| chr2:171793624-171793899 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:171826795-171826944 | Rare:38 | ||||
| chr2:171983069-171983207 | Common:2; Rare:20 | ||||
| chr2:172283042-172283219 | Common:2; Rare:35 |