| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152099038-152099134 | Rare:45; Clinvar (benign):1 | ||||
| chr2:152175678-152176049 | Common:2; Rare:102 | ||||
| chr2:152717829-152717972 | Rare:61 | ||||
| chr2:152717995-152718315 | Common:1; Rare:106 | ||||
| chr2:152718490-152718660 | Rare:68 | ||||
| chr2:156332677-156332904 | Rare:70; Clinvar:2 | ||||
| chr2:156436151-156436450 | Common:3; Rare:94 | ||||
| chr2:158968442-158968685 | Rare:75 | ||||
| chr2:159286607-159286893 | Common:5; Rare:102 | ||||
| chr2:159615214-159615336 | Common:2; Rare:28 | ||||
| chr2:159615551-159615696 | Common:1; Rare:48 | ||||
| chr2:159616427-159616624 | Common:2; Rare:40 | ||||
| chr2:159712340-159712606 | Common:2; Rare:96 | ||||
| chr2:160062469-160062750 | Common:6; Rare:71 | ||||
| chr2:161308355-161308533 | Common:2; Rare:46 |