| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237627295-237627662 | Common:3; Rare:113 | ||||
| chr2:237966743-237967078 | Common:4; Rare:107 | ||||
| chr2:238060728-238061069 | Common:4; Rare:108 | ||||
| chr2:238203583-238203797 | Common:3; Rare:88 | ||||
| chr2:238426892-238427067 | Common:1; Rare:65 | ||||
| chr2:239401641-239401781 | Rare:72 | ||||
| chr2:240025282-240025488 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240136232-240136561 | Common:2; Rare:124 | ||||
| chr2:240560766-240560888 | Common:2; Rare:54 | ||||
| chr2:240561060-240561326 | Common:4; Rare:118 | ||||
| chr2:241102269-241102508 | Common:2; Rare:72 | ||||
| chr2:241272798-241272964 | Rare:67 | ||||
| chr2:241315122-241315477 | Common:6; Rare:116 | ||||
| chr2:241315644-241315997 | Common:5; Rare:137 | ||||
| chr2:241508479-241508913 | Common:2; Rare:139 |