| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237414013-237414407 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr2:237487169-237487310 | Common:1; Rare:42 | ||||
| chr2:237966761-237967078 | Common:4; Rare:97 | ||||
| chr2:238203583-238203805 | Common:3; Rare:92 | ||||
| chr2:238426879-238427083 | Common:1; Rare:75 | ||||
| chr2:240025282-240025477 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240560756-240560873 | Common:1; Rare:51 | ||||
| chr2:241102255-241102495 | Common:2; Rare:77 | ||||
| chr2:241149445-241149568 | Common:1; Rare:35 | ||||
| chr2:241239757-241239935 | Rare:64 | ||||
| chr2:241272778-241272988 | Rare:76 | ||||
| chr2:241315114-241315414 | Common:5; Rare:105 | ||||
| chr2:241315623-241315989 | Common:5; Rare:140 | ||||
| chr2:241508544-241508855 | Common:2; Rare:95 | ||||
| chr2:241637539-241637717 | Common:1; Rare:98 |