| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:138501652-138502010 | Common:3; Rare:129 | ||||
| chr2:144517460-144517767 | Common:5; Rare:84 | ||||
| chr2:144518134-144518199 | Common:1; Rare:12 | ||||
| chr2:144520054-144520528 | Common:4; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:148020673-148021109 | Common:2; Rare:101; Clinvar (benign):2 | ||||
| chr2:148021329-148021462 | Rare:28 | ||||
| chr2:148021495-148021652 | Rare:37 | ||||
| chr2:149587310-149587401 | Rare:16 | ||||
| chr2:149587663-149587827 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:150485350-150485522 | Common:1; Rare:37 | ||||
| chr2:150487550-150487630 | Rare:9 | ||||
| chr2:151828355-151828793 | Common:3; Rare:131 | ||||
| chr2:152175664-152176073 | Common:2; Rare:120 | ||||
| chr2:152717822-152717947 | Rare:48 | ||||
| chr2:152717970-152718095 | Rare:41 |