| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10448303-10448716 | Common:1; Rare:129 | ||||
| chr2:12718056-12718242 | Common:2; Rare:36 | ||||
| chr2:17753764-17753903 | Common:2; Rare:52 | ||||
| chr2:20051524-20051906 | Common:1; Rare:106 | ||||
| chr2:24076324-24076573 | Rare:67 | ||||
| chr2:24793133-24793452 | Rare:141; Clinvar:1 | ||||
| chr2:24971915-24972136 | Common:1; Rare:72 | ||||
| chr2:26244579-26244956 | Common:2; Rare:137; Clinvar:6; Clinvar (benign):8 | ||||
| chr2:26345789-26346165 | Common:1; Rare:112 | ||||
| chr2:27032894-27033066 | Rare:65 | ||||
| chr2:27040120-27040357 | Common:1; Rare:64 | ||||
| chr2:27078540-27078952 | Common:2; Rare:99 | ||||
| chr2:27212261-27212366 | Common:1; Rare:54 | ||||
| chr2:27356750-27356789 | Rare:7 | ||||
| chr2:27370251-27370676 | Common:1; Rare:172 |