| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135052164-135052323 | Common:1; Rare:58; Clinvar (benign):1 | ||||
| chr2:135531153-135531547 | Common:1; Rare:84 | ||||
| chr2:135985401-135985720 | Common:4; Rare:133; Clinvar (benign):1 | ||||
| chr2:138501581-138501945 | Common:4; Rare:143 | ||||
| chr2:144517337-144517767 | Common:5; Rare:127; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:148020636-148021105 | Common:2; Rare:106; Clinvar (benign):2 | ||||
| chr2:148021480-148021688 | Rare:54; Clinvar (benign):1 | ||||
| chr2:148021736-148021868 | Rare:22 | ||||
| chr2:149587269-149587402 | Common:1; Rare:29 | ||||
| chr2:149587662-149587821 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:150487087-150487180 | Common:6; Rare:22 | ||||
| chr2:152664049-152664218 | Rare:29 | ||||
| chr2:152717831-152718103 | Rare:105 | ||||
| chr2:152718490-152718976 | Common:1; Rare:237; Clinvar:1 | ||||
| chr2:156332670-156332904 | Rare:76; Clinvar:3 |