Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:65227579-65227949 | Rare:100 | ||||
chr2:66434807-66435130 | Common:1; Rare:80 | ||||
chr2:68157456-68157953 | Common:2; Rare:255 | ||||
chr2:68319968-68320062 | Rare:18 | ||||
chr2:68467255-68467688 | Common:2; Rare:120 | ||||
chr2:69387123-69387428 | Rare:90; Clinvar:2 | ||||
chr2:69643597-69643824 | Rare:76 | ||||
chr2:69741849-69742165 | Common:1; Rare:67 | ||||
chr2:69829517-69829737 | Common:1; Rare:87 | ||||
chr2:70086941-70087114 | Rare:85 | ||||
chr2:70087309-70087585 | Common:2; Rare:103 | ||||
chr2:70257902-70258231 | Common:2; Rare:107 | ||||
chr2:70293650-70293841 | Common:2; Rare:66 | ||||
chr2:71068539-71068681 | Rare:61 | ||||
chr2:71130215-71130677 | Common:6; Rare:131; Clinvar:1; Clinvar (benign):2 |