| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237413952-237414582 | Common:3; Rare:125; Clinvar (benign):3 | ||||
| chr2:237487150-237487298 | Common:2; Rare:38 | ||||
| chr2:237966728-237967078 | Common:4; Rare:108 | ||||
| chr2:238060683-238061029 | Common:5; Rare:111 | ||||
| chr2:238203602-238203815 | Common:3; Rare:92 | ||||
| chr2:238426655-238427012 | Common:6; Rare:95 | ||||
| chr2:239401641-239401781 | Rare:72 | ||||
| chr2:240025282-240025455 | Common:1; Rare:69; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240560761-240560873 | Common:1; Rare:48 | ||||
| chr2:241102276-241102442 | Common:2; Rare:49 | ||||
| chr2:241230159-241230346 | Rare:52 | ||||
| chr2:241240007-241240362 | Common:1; Rare:87 | ||||
| chr2:241272770-241273017 | Rare:83 | ||||
| chr2:241315114-241315440 | Common:5; Rare:113 | ||||
| chr2:241315641-241316186 | Common:5; Rare:200 |