Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74529406-74530021 | Common:1; Rare:213; Clinvar:5; Clinvar (benign):3 | ||||
chr2:74958872-74959021 | Rare:57 | ||||
chr2:75710660-75710778 | Common:2; Rare:47 | ||||
chr2:84459221-84459572 | Common:3; Rare:90; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:85327945-85328080 | Common:2; Rare:63 | ||||
chr2:85354501-85354807 | Common:1; Rare:105 | ||||
chr2:85413983-85414106 | Common:1; Rare:27 | ||||
chr2:85539072-85539195 | Common:2; Rare:54 | ||||
chr2:85561443-85561581 | Rare:52; Clinvar:4 | ||||
chr2:85595558-85595769 | Common:1; Rare:68 | ||||
chr2:85602660-85602892 | Rare:58 | ||||
chr2:85612007-85612104 | Rare:35 | ||||
chr2:86105837-86106183 | Common:2; Rare:88 | ||||
chr2:86195348-86195522 | Common:3; Rare:61 | ||||
chr2:86441174-86441500 | Common:2; Rare:123 |