Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:186806447-186806556 | Rare:35 | ||||
chr3:187139451-187139558 | Rare:43 | ||||
chr3:188153761-188153885 | Common:1; Rare:22 | ||||
chr3:188154060-188154227 | Rare:53 | ||||
chr3:192917840-192918006 | Common:2; Rare:75 | ||||
chr3:193593101-193593380 | Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
chr3:194632842-194632946 | Rare:15 | ||||
chr3:195584103-195584405 | Common:12; Rare:61 | ||||
chr3:196318149-196318352 | Common:1; Rare:87 | ||||
chr3:196503689-196503945 | Common:5; Rare:87 | ||||
chr3:196712213-196712311 | Common:1; Rare:33 | ||||
chr3:196867748-196867931 | Rare:57 | ||||
chr3:196942368-196942659 | Common:1; Rare:119 | ||||
chr3:197029778-197029966 | Common:1; Rare:60 | ||||
chr3:197749830-197749979 | Rare:65 |