Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74385591-74385779 | Rare:29 | ||||
chr2:74391792-74392082 | Common:2; Rare:148 | ||||
chr2:74421480-74421794 | Rare:93 | ||||
chr2:74440487-74440619 | Rare:42 | ||||
chr2:74458065-74458504 | Common:1; Rare:136 | ||||
chr2:74465354-74465487 | Common:1; Rare:39 | ||||
chr2:74482937-74483121 | Common:1; Rare:72 | ||||
chr2:74507262-74507480 | Rare:56 | ||||
chr2:74507667-74507785 | Rare:25 | ||||
chr2:74529607-74529799 | Rare:83; Clinvar:2 | ||||
chr2:74529856-74530202 | Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74554388-74554727 | Common:1; Rare:96 | ||||
chr2:74654103-74654396 | Common:1; Rare:103 | ||||
chr2:74958530-74958707 | Common:4; Rare:67 | ||||
chr2:75199518-75199641 | Rare:22 |