Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:49132836-49133083 | Rare:57; Clinvar:2 | ||||
chr3:49166289-49166417 | Common:1; Rare:34 | ||||
chr3:49339996-49340127 | Common:2; Rare:62 | ||||
chr3:49358247-49358486 | Common:3; Rare:128 | ||||
chr3:49411870-49412213 | Common:1; Rare:117 | ||||
chr3:49469997-49470303 | Common:1; Rare:88 | ||||
chr3:49674228-49674397 | Common:1; Rare:64 | ||||
chr3:49689459-49689609 | Rare:47 | ||||
chr3:49723922-49724238 | Common:9; Rare:116 | ||||
chr3:50267535-50267659 | Rare:51 | ||||
chr3:50299329-50299681 | Common:1; Rare:87 | ||||
chr3:50328163-50328353 | Rare:58 | ||||
chr3:50350714-50350897 | Common:1; Rare:27 | ||||
chr3:50351034-50351210 | Common:3; Rare:32 | ||||
chr3:50569400-50569527 | Rare:28 |