Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633917-49634043 | Common:1; Rare:57; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49862639-49863007 | Common:1; Rare:169 | ||||
chr14:49993082-49993261 | Rare:26 | ||||
chr14:49999276-49999370 | Rare:21 | ||||
chr14:50000084-50000297 | Common:2; Rare:37 | ||||
chr14:50000882-50001089 | Rare:39 | ||||
chr14:50001247-50001414 | Common:2; Rare:34 | ||||
chr14:50040545-50040702 | Rare:23 | ||||
chr14:50062733-50062904 | Common:2; Rare:24 | ||||
chr14:51396259-51396650 | Common:2; Rare:83 | ||||
chr14:51397158-51397298 | Common:1; Rare:35 | ||||
chr14:54773240-54773333 | Rare:22 | ||||
chr14:55103327-55103412 | Rare:21 | ||||
chr14:61103616-61103654 | Rare:7 | ||||
chr14:61178788-61178964 | Common:2; Rare:28 |