| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152175882-152176121 | Common:1; Rare:59 | ||||
| chr2:152717829-152717972 | Rare:61 | ||||
| chr2:152718473-152718650 | Rare:67 | ||||
| chr2:153478656-153478963 | Common:2; Rare:80 | ||||
| chr2:156332675-156332904 | Rare:72; Clinvar:3 | ||||
| chr2:156436118-156436404 | Common:3; Rare:85 | ||||
| chr2:158968476-158968702 | Rare:72 | ||||
| chr2:159615207-159615314 | Common:3; Rare:22 | ||||
| chr2:159615576-159615659 | Common:1; Rare:26 | ||||
| chr2:159616402-159616830 | Common:2; Rare:75 | ||||
| chr2:159712351-159712625 | Common:2; Rare:101 | ||||
| chr2:161160587-161160796 | Rare:50 | ||||
| chr2:161308325-161308579 | Common:2; Rare:63 | ||||
| chr2:161416100-161416520 | Rare:77; Clinvar (benign):1 | ||||
| chr2:161416564-161416774 | Rare:48 |