Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:61279368-61279416 | Rare:12 | ||||
chr14:61721321-61721784 | Common:1; Rare:97 | ||||
chr14:61724048-61724052 | Rare:1 | ||||
chr14:61744490-61744720 | Common:2; Rare:45 | ||||
chr14:64427127-64427451 | Common:1; Rare:63 | ||||
chr14:68898210-68898364 | Common:1; Rare:24 | ||||
chr14:68901833-68901961 | Common:3; Rare:24 | ||||
chr14:69886145-69886198 | Rare:6 | ||||
chr14:74502759-74503102 | Rare:102; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:74503217-74503528 | Common:2; Rare:114; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:74538717-74539043 | Common:1; Rare:54 | ||||
chr14:74551938-74552367 | Common:3; Rare:127; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:81219361-81219525 | Rare:34 | ||||
chr14:95516610-95516772 | Common:2; Rare:37 | ||||
chr14:96039200-96039382 | Common:2; Rare:50 |