Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:45764797-45765083 | Common:2; Rare:51 | ||||
chr14:48702560-48702626 | Rare:16 | ||||
chr14:49621701-49621772 | Rare:22 | ||||
chr14:49621779-49621917 | Rare:43; Clinvar (benign):1 | ||||
chr14:49622077-49622274 | Rare:59; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr14:49622336-49622873 | Rare:123; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49622929-49623333 | Common:1; Rare:77; Clinvar:4 | ||||
chr14:49633938-49634098 | Common:1; Rare:73; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49634268-49634500 | Common:1; Rare:112; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49637695-49638004 | Common:1; Rare:50 | ||||
chr14:49797259-49797327 | Common:1; Rare:7 | ||||
chr14:49799435-49799542 | Common:1; Rare:33 | ||||
chr14:49851567-49851850 | Common:1; Rare:89 | ||||
chr14:49862873-49862985 | Rare:44 | ||||
chr14:49982498-49982828 | Common:2; Rare:60 |