Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:144520053-144520483 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr2:148020681-148021109 | Common:2; Rare:99; Clinvar (benign):2 | ||||
chr2:148021135-148021464 | Rare:75 | ||||
chr2:148021547-148021658 | Rare:21 | ||||
chr2:149587310-149587348 | Rare:6 | ||||
chr2:149587685-149587821 | Common:1; Rare:38; Clinvar:1 | ||||
chr2:152717821-152717964 | Rare:57 | ||||
chr2:152717995-152718288 | Common:1; Rare:95 | ||||
chr2:152718458-152718641 | Rare:64 | ||||
chr2:156332712-156332870 | Rare:48; Clinvar:2 | ||||
chr2:156436118-156436427 | Common:3; Rare:93 | ||||
chr2:157875794-157876133 | Common:1; Rare:102 | ||||
chr2:158968507-158968715 | Rare:64 | ||||
chr2:159286690-159286906 | Common:5; Rare:85 | ||||
chr2:159615225-159615302 | Common:2; Rare:18 |