| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:236507420-236507639 | Common:6; Rare:76 | ||||
| chr2:237085748-237085951 | Common:2; Rare:74 | ||||
| chr2:237487128-237487323 | Common:3; Rare:53 | ||||
| chr2:238060745-238061090 | Common:6; Rare:106 | ||||
| chr2:238203583-238203797 | Common:3; Rare:88 | ||||
| chr2:238426676-238427067 | Common:6; Rare:116 | ||||
| chr2:238847887-238848190 | Common:1; Rare:73 | ||||
| chr2:240025282-240025480 | Common:1; Rare:78; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136232-240136382 | Rare:61 | ||||
| chr2:240560766-240560873 | Common:1; Rare:46 | ||||
| chr2:240561036-240561258 | Common:2; Rare:93 | ||||
| chr2:241102263-241102442 | Common:2; Rare:57 | ||||
| chr2:241272789-241272976 | Rare:72 | ||||
| chr2:241315149-241315326 | Common:3; Rare:63 | ||||
| chr2:241315646-241315989 | Common:5; Rare:133 |