Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:677002-677185 | Rare:50 | ||||
chr2:677338-677518 | Common:1; Rare:74 | ||||
chr2:950704-950908 | Common:3; Rare:70 | ||||
chr2:3377691-3378016 | Common:1; Rare:96 | ||||
chr2:3379587-3379732 | Common:2; Rare:47 | ||||
chr2:3519485-3519674 | Common:3; Rare:56 | ||||
chr2:3558147-3558762 | Common:6; Rare:215 | ||||
chr2:3575092-3575384 | Common:2; Rare:86; Clinvar:3; Clinvar (benign):6 | ||||
chr2:5692125-5692409 | Rare:65 | ||||
chr2:5693017-5693377 | Common:1; Rare:123; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr2:6917296-6917498 | Rare:72 | ||||
chr2:8682484-8682599 | Rare:39 | ||||
chr2:8837492-8837734 | Common:1; Rare:90 | ||||
chr2:9003648-9004067 | Common:2; Rare:130 | ||||
chr2:9206653-9206861 | Rare:66 |