Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74958736-74958815 | Rare:35 | ||||
chr2:74958870-74959080 | Rare:74 | ||||
chr2:75710669-75710793 | Common:2; Rare:54 | ||||
chr2:75710864-75711055 | Common:1; Rare:67 | ||||
chr2:84459180-84459582 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:84905544-84905689 | Common:1; Rare:44 | ||||
chr2:85328081-85328359 | Common:6; Rare:66 | ||||
chr2:85354564-85354807 | Common:1; Rare:75 | ||||
chr2:85538718-85538868 | Common:2; Rare:41 | ||||
chr2:85539019-85539373 | Common:3; Rare:169; Clinvar (benign):7 | ||||
chr2:85561432-85561581 | Rare:56; Clinvar:4 | ||||
chr2:85595546-85595762 | Common:2; Rare:64 | ||||
chr2:85602639-85602890 | Rare:65 | ||||
chr2:85612025-85612171 | Rare:40 | ||||
chr2:86195391-86195541 | Common:5; Rare:54 |