Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75985694-75985798 | Rare:44; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr14:76310262-76310606 | Common:3; Rare:68 | ||||
chr14:76310612-76310788 | Common:2; Rare:24 | ||||
chr14:76762648-76762956 | Rare:98 | ||||
chr14:77098048-77098364 | Rare:91 | ||||
chr14:77320838-77321060 | Rare:65; Clinvar:1 | ||||
chr14:77376976-77377425 | Common:5; Rare:133 | ||||
chr14:77457542-77457881 | Common:1; Rare:100 | ||||
chr14:77457997-77458151 | Rare:43 | ||||
chr14:77707991-77708182 | Common:2; Rare:100 | ||||
chr14:81220708-81221069 | Common:3; Rare:141 | ||||
chr14:81221264-81221404 | Common:1; Rare:24 | ||||
chr14:81436403-81436613 | Common:4; Rare:80 | ||||
chr14:85529860-85530233 | Common:2; Rare:77 | ||||
chr14:88551451-88551609 | Common:2; Rare:37 |