| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190648709-190648922 | Common:1; Rare:77 | ||||
| chr2:190649464-190649602 | Common:1; Rare:39 | ||||
| chr2:190880626-190880834 | Common:3; Rare:63 | ||||
| chr2:191014133-191014353 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191150938-191151310 | Common:1; Rare:65 | ||||
| chr2:191245231-191245487 | Common:2; Rare:84 | ||||
| chr2:191246126-191246339 | Common:1; Rare:61 | ||||
| chr2:191677854-191678188 | Common:4; Rare:96 | ||||
| chr2:191846903-191847099 | Rare:57 | ||||
| chr2:191847106-191847157 | Rare:9 | ||||
| chr2:191847173-191847299 | Rare:18 | ||||
| chr2:196068825-196068915 | Common:1; Rare:22 | ||||
| chr2:196593518-196593738 | Common:1; Rare:57 | ||||
| chr2:196799583-196799787 | Common:1; Rare:67 | ||||
| chr2:196926689-196927014 | Common:4; Rare:109 |