| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:149038644-149038754 | Common:1; Rare:39 | ||||
| chr2:149587310-149587364 | Rare:10 | ||||
| chr2:149587672-149587832 | Common:1; Rare:47; Clinvar:1 | ||||
| chr2:150485382-150485503 | Rare:30 | ||||
| chr2:150487054-150487275 | Common:6; Rare:48 | ||||
| chr2:152098729-152099098 | Common:1; Rare:120; Clinvar:6; Clinvar (benign):6 | ||||
| chr2:152175681-152176048 | Common:2; Rare:101 | ||||
| chr2:152335026-152335174 | Common:1; Rare:56 | ||||
| chr2:152717829-152717994 | Rare:71 | ||||
| chr2:152718473-152718643 | Rare:63 | ||||
| chr2:153478754-153478947 | Common:1; Rare:55 | ||||
| chr2:156332679-156332870 | Rare:55; Clinvar:2 | ||||
| chr2:156436276-156436459 | Common:3; Rare:54 | ||||
| chr2:158968516-158968688 | Rare:52 | ||||
| chr2:159286581-159286867 | Common:4; Rare:103 |