Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:59368436-59368763 | Common:2; Rare:72; Clinvar:1 | ||||
chr14:60797979-60798100 | Rare:31 | ||||
chr14:61751024-61751168 | Rare:37 | ||||
chr14:63891251-63891295 | Rare:11 | ||||
chr14:63891372-63891405 | Rare:10 | ||||
chr14:64415413-64415735 | Common:1; Rare:78; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:64442087-64442292 | Common:1; Rare:57; Clinvar (benign):1 | ||||
chr14:65413723-65413792 | Common:1; Rare:14 | ||||
chr14:67615597-67615628 | Common:1; Rare:9 | ||||
chr14:69151521-69151823 | Common:2; Rare:80 | ||||
chr14:69385438-69385494 | Rare:9 | ||||
chr14:70187058-70187157 | Rare:35 | ||||
chr14:70255463-70255667 | Common:6; Rare:73 | ||||
chr14:70293941-70294229 | Common:6; Rare:54 | ||||
chr14:70342662-70342917 | Common:1; Rare:49 |