Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:34982245-34982321 | Common:3; Rare:23 | ||||
chr14:34982352-34982763 | Common:1; Rare:159 | ||||
chr14:34982888-34983138 | Common:5; Rare:89 | ||||
chr14:35045941-35046554 | Common:2; Rare:182 | ||||
chr14:35046577-35046726 | Common:2; Rare:57 | ||||
chr14:35046859-35046953 | Common:1; Rare:21 | ||||
chr14:35047116-35047175 | Common:1; Rare:13 | ||||
chr14:35121676-35121881 | Rare:52 | ||||
chr14:35121897-35122135 | Common:2; Rare:73 | ||||
chr14:35122204-35122804 | Common:2; Rare:168 | ||||
chr14:35122985-35123301 | Common:1; Rare:83 | ||||
chr14:35291913-35292011 | Rare:25 | ||||
chr14:35292046-35292543 | Common:7; Rare:140; Clinvar:1 | ||||
chr14:35403688-35404094 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):3 | ||||
chr14:35404383-35404836 | Common:3; Rare:149; Clinvar:1; Clinvar (benign):5 |