Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49586327-49586772 | Common:1; Rare:237; Clinvar (benign):1 | ||||
chr14:49598731-49598996 | Rare:98 | ||||
chr14:49620573-49620820 | Common:2; Rare:98; Clinvar:1 | ||||
chr14:49688182-49688287 | Rare:41 | ||||
chr14:49693022-49693167 | Common:1; Rare:47 | ||||
chr14:49892774-49893125 | Common:1; Rare:143 | ||||
chr14:50312179-50312374 | Rare:80 | ||||
chr14:50532461-50532744 | Common:3; Rare:88 | ||||
chr14:50561123-50561141 | Rare:2 | ||||
chr14:50668346-50668556 | Common:3; Rare:82 | ||||
chr14:50944405-50944782 | Common:7; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51240107-51240312 | Common:1; Rare:90 | ||||
chr14:51651670-51651983 | Common:4; Rare:90 | ||||
chr14:51989380-51989642 | Common:2; Rare:85 | ||||
chr14:52069000-52069224 | Common:2; Rare:50 |