Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20343167-20343644 | Common:13; Rare:280 | ||||
chr14:20413413-20413538 | Common:3; Rare:37 | ||||
chr14:20454762-20455320 | Common:7; Rare:145 | ||||
chr14:20455376-20455698 | Rare:88 | ||||
chr14:20683920-20684244 | Common:19; Rare:158; Clinvar:1; Clinvar (benign):2 | ||||
chr14:20684427-20684745 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):3 | ||||
chr14:20802795-20802970 | Common:1; Rare:23 | ||||
chr14:20955410-20955492 | Common:1; Rare:12 | ||||
chr14:20989665-20990057 | Common:7; Rare:100 | ||||
chr14:20999078-20999305 | Rare:44 | ||||
chr14:21022062-21022441 | Rare:98 | ||||
chr14:21024987-21025191 | Rare:75 | ||||
chr14:21025682-21025806 | Rare:24 | ||||
chr14:21269274-21269328 | Rare:10 | ||||
chr14:21456035-21456453 | Common:4; Rare:108 |