| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:152718489-152718639 | Rare:56 | ||||
| chr2:153478656-153478953 | Common:2; Rare:79 | ||||
| chr2:156332682-156332904 | Rare:68; Clinvar:2 | ||||
| chr2:156436263-156436410 | Common:3; Rare:50 | ||||
| chr2:158456649-158456948 | Common:1; Rare:107 | ||||
| chr2:158968475-158968685 | Rare:65 | ||||
| chr2:159286638-159286893 | Common:5; Rare:96 | ||||
| chr2:159516523-159516665 | Common:1; Rare:16 | ||||
| chr2:159615225-159615343 | Common:2; Rare:28 | ||||
| chr2:159615556-159615696 | Common:1; Rare:46 | ||||
| chr2:159616427-159616690 | Common:2; Rare:50 | ||||
| chr2:159712343-159712584 | Common:2; Rare:91 | ||||
| chr2:161308320-161308514 | Common:2; Rare:51 | ||||
| chr2:161415890-161416094 | Common:1; Rare:35 | ||||
| chr2:161416100-161416501 | Rare:75; Clinvar (benign):1 |