Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35402167-35402621 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):2 | ||||
chr14:39388724-39388906 | Rare:37 | ||||
chr14:49621844-49621949 | Rare:32; Clinvar (benign):1 | ||||
chr14:49633854-49634064 | Common:1; Rare:76; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:49640878-49641063 | Rare:29 | ||||
chr14:49789506-49789743 | Rare:55 | ||||
chr14:49862614-49863036 | Common:1; Rare:191 | ||||
chr14:49868149-49868453 | Common:3; Rare:64 | ||||
chr14:49924059-49924121 | Rare:15 | ||||
chr14:50003383-50003545 | Common:1; Rare:43 | ||||
chr14:53613709-53614090 | Rare:76 | ||||
chr14:55103185-55103208 | Rare:2 | ||||
chr14:55129847-55129894 | Rare:10 | ||||
chr14:55130034-55130339 | Rare:50 | ||||
chr14:55133657-55133992 | Common:4; Rare:60 |