| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:217905450-217905614 | Rare:34 | ||||
| chr2:217919840-217920149 | Common:3; Rare:61 | ||||
| chr2:217978639-217978734 | Rare:29 | ||||
| chr2:217978773-217978943 | Common:1; Rare:50 | ||||
| chr2:218217046-218217254 | Common:1; Rare:72 | ||||
| chr2:218217446-218217630 | Common:2; Rare:65 | ||||
| chr2:218269489-218269669 | Rare:72 | ||||
| chr2:218270041-218270586 | Common:5; Rare:176; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218271205-218271544 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:218280009-218280245 | Rare:68 | ||||
| chr2:218287270-218287395 | Rare:20 | ||||
| chr2:218289992-218290044 | Common:1; Rare:7 | ||||
| chr2:218292470-218292657 | Common:1; Rare:57 | ||||
| chr2:218323010-218323355 | Common:6; Rare:117 | ||||
| chr2:218339797-218340088 | Common:3; Rare:101; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 |