Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:30147843-30147965 | Common:1; Rare:45 | ||||
chr2:30231278-30231639 | Common:1; Rare:110 | ||||
chr2:32009956-32010145 | Common:1; Rare:61 | ||||
chr2:32010963-32011087 | Rare:33 | ||||
chr2:32039738-32039860 | Rare:37 | ||||
chr2:32165737-32165898 | Common:1; Rare:61 | ||||
chr2:32277765-32277981 | Common:1; Rare:55 | ||||
chr2:32628017-32628128 | Rare:35 | ||||
chr2:33134236-33134959 | Common:4; Rare:167 | ||||
chr2:33599202-33599580 | Common:1; Rare:133 | ||||
chr2:36966600-36966830 | Common:3; Rare:93 | ||||
chr2:37084269-37084561 | Common:4; Rare:110 | ||||
chr2:37231418-37231722 | Common:5; Rare:153; Clinvar (benign):3 | ||||
chr2:37671431-37671782 | Common:2; Rare:125 | ||||
chr2:37672495-37672719 | Common:5; Rare:74 |