Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:74483198-74483387 | Common:1; Rare:69 | ||||
chr2:74503321-74503475 | Rare:39 | ||||
chr2:74507262-74507500 | Rare:62 | ||||
chr2:74507653-74507861 | Rare:51 | ||||
chr2:74529653-74530189 | Rare:165; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74530434-74530638 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74553941-74554083 | Rare:23 | ||||
chr2:74554388-74554755 | Common:2; Rare:110 | ||||
chr2:74555624-74555798 | Common:1; Rare:50 | ||||
chr2:74654081-74654311 | Common:1; Rare:60 | ||||
chr2:74833859-74834169 | Rare:91 | ||||
chr2:74834819-74835026 | Rare:55 | ||||
chr2:74835132-74835298 | Rare:43 | ||||
chr2:74958388-74958782 | Common:7; Rare:136 | ||||
chr2:74958872-74959076 | Rare:73 |