Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24213064-24213198 | Rare:26 | ||||
chr14:24213425-24213529 | Rare:37 | ||||
chr14:24232285-24232975 | Common:9; Rare:171 | ||||
chr14:24233147-24233269 | Common:1; Rare:36 | ||||
chr14:24235547-24235776 | Common:1; Rare:51 | ||||
chr14:24238087-24238357 | Common:2; Rare:80 | ||||
chr14:24242276-24242429 | Rare:50; Clinvar (benign):2 | ||||
chr14:24242562-24242774 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24271453-24271774 | Common:2; Rare:94 | ||||
chr14:24299691-24299862 | Common:4; Rare:48 | ||||
chr14:24309780-24310058 | Common:1; Rare:55 | ||||
chr14:24314761-24314934 | Rare:26 | ||||
chr14:24335050-24335372 | Common:3; Rare:64 | ||||
chr14:24429836-24430342 | Common:5; Rare:123 | ||||
chr14:24430938-24431108 | Common:2; Rare:50 |