Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:219567542-219567787 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr2:223943825-223944233 | Common:1; Rare:85 | ||||
chr2:227606510-227606798 | Common:6; Rare:53 | ||||
chr2:227655548-227655830 | Rare:50 | ||||
chr2:227671714-227671982 | Common:3; Rare:42 | ||||
chr2:227674438-227674779 | Common:1; Rare:53 | ||||
chr2:227704188-227704298 | Common:1; Rare:21 | ||||
chr2:227713291-227713550 | Common:4; Rare:27 | ||||
chr2:227805798-227806069 | Common:3; Rare:63 | ||||
chr2:227818207-227818503 | Common:2; Rare:45 | ||||
chr2:227863359-227863572 | Rare:50 | ||||
chr2:227877450-227877565 | Rare:25 | ||||
chr2:231514362-231514583 | Common:5; Rare:88 | ||||
chr2:231604596-231604927 | Common:21; Rare:116 | ||||
chr2:231614154-231614494 | Common:7; Rare:82 |