| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148021553-148021658 | Rare:20 | ||||
| chr2:149330358-149330597 | Common:1; Rare:102 | ||||
| chr2:149587093-149587400 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:149587674-149587884 | Common:1; Rare:59; Clinvar:1 | ||||
| chr2:150485382-150485528 | Rare:33 | ||||
| chr2:151289619-151289947 | Common:1; Rare:66 | ||||
| chr2:151410050-151410161 | Rare:37 | ||||
| chr2:151828459-151828793 | Common:2; Rare:95 | ||||
| chr2:152175454-152175540 | Rare:23 | ||||
| chr2:152175882-152176099 | Common:1; Rare:58 | ||||
| chr2:152717829-152717964 | Rare:56 | ||||
| chr2:152717991-152718288 | Common:1; Rare:96 | ||||
| chr2:152718450-152718670 | Rare:88 | ||||
| chr2:156332673-156332904 | Rare:73; Clinvar:3 | ||||
| chr2:156436118-156436440 | Common:3; Rare:96 |