| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:149587172-149587656 | Common:3; Rare:101; Clinvar (benign):1 | ||||
| chr2:149587685-149587822 | Common:1; Rare:39; Clinvar:1 | ||||
| chr2:152175694-152175792 | Rare:30 | ||||
| chr2:152175888-152176142 | Common:1; Rare:62 | ||||
| chr2:152335362-152335655 | Rare:100 | ||||
| chr2:152664184-152664424 | Common:2; Rare:49 | ||||
| chr2:152717829-152717935 | Rare:45 | ||||
| chr2:152717947-152718297 | Common:1; Rare:120 | ||||
| chr2:152718473-152718644 | Rare:64 | ||||
| chr2:156436098-156436440 | Common:3; Rare:99 | ||||
| chr2:158457772-158457917 | Common:1; Rare:43 | ||||
| chr2:159516523-159516648 | Common:1; Rare:14 | ||||
| chr2:159615434-159615658 | Common:2; Rare:73 | ||||
| chr2:159712153-159712270 | Common:1; Rare:42 | ||||
| chr2:159712326-159712600 | Common:2; Rare:100 |