Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:23435614-23435947 | Common:2; Rare:62 | ||||
chr14:23555941-23556096 | Common:1; Rare:44 | ||||
chr14:23556208-23556348 | Common:2; Rare:31 | ||||
chr14:23567756-23567843 | Rare:23 | ||||
chr14:23953661-23953810 | Common:6; Rare:53 | ||||
chr14:23988775-23988930 | Common:8; Rare:62 | ||||
chr14:24114921-24115319 | Common:2; Rare:113 | ||||
chr14:24135953-24136299 | Common:1; Rare:110 | ||||
chr14:24141577-24141862 | Common:1; Rare:61 | ||||
chr14:24146582-24146740 | Rare:53 | ||||
chr14:24195403-24195744 | Common:1; Rare:76 | ||||
chr14:24232295-24232707 | Common:8; Rare:104 | ||||
chr14:24232832-24232961 | Rare:30 | ||||
chr14:24242264-24242367 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24263159-24263303 | Common:2; Rare:36 |