Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24429838-24430070 | Common:2; Rare:52 | ||||
chr14:24430438-24430579 | Rare:22 | ||||
chr14:24442659-24443043 | Common:5; Rare:121 | ||||
chr14:31420527-31420755 | Common:3; Rare:69 | ||||
chr14:32076807-32077022 | Common:3; Rare:80 | ||||
chr14:34982479-34982656 | Common:1; Rare:76 | ||||
chr14:35046624-35046702 | Common:1; Rare:32 | ||||
chr14:35121925-35122597 | Common:3; Rare:197 | ||||
chr14:44961896-44962203 | Common:2; Rare:86 | ||||
chr14:49598664-49598961 | Common:1; Rare:114 | ||||
chr14:49620596-49620817 | Common:2; Rare:76; Clinvar:1 | ||||
chr14:50312153-50312379 | Rare:100 | ||||
chr14:50532449-50532787 | Common:4; Rare:109 | ||||
chr14:50944322-50944631 | Common:4; Rare:113; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:51651664-51651994 | Common:4; Rare:95 |