Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24141577-24141862 | Common:1; Rare:61 | ||||
chr14:24144192-24144461 | Common:2; Rare:70 | ||||
chr14:24146553-24146737 | Rare:67 | ||||
chr14:24147252-24147480 | Common:2; Rare:59 | ||||
chr14:24195393-24195728 | Common:2; Rare:73 | ||||
chr14:24213065-24213188 | Rare:22 | ||||
chr14:24213413-24213539 | Rare:46 | ||||
chr14:24213542-24213606 | Common:1; Rare:16 | ||||
chr14:24232312-24232776 | Common:8; Rare:107 | ||||
chr14:24232823-24232961 | Common:1; Rare:31 | ||||
chr14:24242272-24242413 | Rare:48; Clinvar (benign):1 | ||||
chr14:24242539-24242770 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):3 | ||||
chr14:24299706-24299890 | Common:4; Rare:58 | ||||
chr14:24442755-24443056 | Common:5; Rare:82 | ||||
chr14:30559047-30559191 | Common:2; Rare:50 |