| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178413738-178413981 | Common:1; Rare:73 | ||||
| chr2:189575205-189575561 | Rare:79 | ||||
| chr2:190915737-190915843 | Common:1; Rare:16 | ||||
| chr2:190950660-190950740 | Rare:17 | ||||
| chr2:190951160-190951352 | Rare:35 | ||||
| chr2:197488435-197488721 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197489202-197489462 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr2:199459420-199459766 | Common:2; Rare:107 | ||||
| chr2:200419055-200419310 | Common:1; Rare:46 | ||||
| chr2:202376101-202376342 | Rare:106 | ||||
| chr2:206085160-206085267 | Common:1; Rare:24 | ||||
| chr2:207742903-207743099 | Rare:32 | ||||
| chr2:218277008-218277289 | Common:1; Rare:65 | ||||
| chr2:218344515-218344828 | Common:1; Rare:94; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:218402616-218402714 | Rare:37 |