Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:238404590-238404800 | Common:2; Rare:57 | ||||
chr2:238864200-238864590 | Common:4; Rare:181 | ||||
chr2:240020956-240021751 | Common:2; Rare:351; Clinvar:6; Clinvar (benign):8 | ||||
chr2:240256010-240256260 | Rare:87 | ||||
chr2:240566404-240566804 | Common:13; Rare:217 | ||||
chr2:240857340-240857760 | Common:5; Rare:136 | ||||
chr2:240874042-240874442 | Common:15; Rare:174; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr2:240888690-240889400 | Common:26; Rare:195 | ||||
chr2:240960640-240961020 | Common:8; Rare:137 | ||||
chr2:240967357-240967660 | Common:2; Rare:130 | ||||
chr2:241081294-241081536 | Common:3; Rare:58 | ||||
chr2:241461361-241461526 | Common:1; Rare:27 | ||||
chr2:241552034-241552446 | Common:8; Rare:215 | ||||
chr2:241553565-241553798 | Common:2; Rare:122 | ||||
chr2:241610180-241610520 | Common:1; Rare:122 |