| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237487132-237487431 | Common:3; Rare:76 | ||||
| chr2:237509851-237510112 | Rare:48 | ||||
| chr2:237540490-237540842 | Common:2; Rare:106 | ||||
| chr2:237591093-237591190 | Common:1; Rare:34 | ||||
| chr2:237966715-237967083 | Common:5; Rare:115 | ||||
| chr2:238060728-238061057 | Common:4; Rare:105 | ||||
| chr2:238203543-238203808 | Common:5; Rare:103 | ||||
| chr2:238290055-238290457 | Common:1; Rare:86 | ||||
| chr2:238426655-238427073 | Common:6; Rare:123 | ||||
| chr2:239401640-239401739 | Rare:46 | ||||
| chr2:240025225-240025452 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 | ||||
| chr2:240561036-240561326 | Common:4; Rare:133 | ||||
| chr2:241102260-241102517 | Common:2; Rare:79 | ||||
| chr2:241149434-241149632 | Common:3; Rare:64 |