Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73568049-73568129 | Rare:23 | ||||
chr14:73568999-73569294 | Rare:66 | ||||
chr14:73592015-73592167 | Common:2; Rare:59 | ||||
chr14:73644863-73645041 | Common:3; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
chr14:73787110-73787379 | Common:3; Rare:92 | ||||
chr14:73851739-73852003 | Common:5; Rare:89 | ||||
chr14:73886778-73886897 | Common:2; Rare:40 | ||||
chr14:73950027-73950351 | Common:6; Rare:143; Clinvar (benign):5 | ||||
chr14:74019233-74019467 | Common:1; Rare:89 | ||||
chr14:74084397-74084987 | Common:9; Rare:172 | ||||
chr14:74493193-74493841 | Common:4; Rare:220; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:74611544-74611620 | Rare:22 | ||||
chr14:74612162-74612352 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
chr14:74612367-74612413 | Rare:5 | ||||
chr14:74612559-74612804 | Common:1; Rare:64 |