Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:47243170-47243392 | Rare:53 | ||||
chr14:49633949-49634084 | Common:1; Rare:59; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862626-49863020 | Common:1; Rare:177 | ||||
chr14:50335377-50335589 | Common:1; Rare:70 | ||||
chr14:56120416-56120664 | Common:2; Rare:52 | ||||
chr14:56808446-56808650 | Common:1; Rare:47 | ||||
chr14:56884771-56884807 | Common:1; Rare:4 | ||||
chr14:60248027-60248145 | Rare:25 | ||||
chr14:61751057-61751219 | Rare:40 | ||||
chr14:62118557-62118617 | Common:1; Rare:10 | ||||
chr14:64186242-64186360 | Rare:28 | ||||
chr14:68628383-68628426 | Rare:11 | ||||
chr14:68795244-68795509 | Common:4; Rare:63 | ||||
chr14:69886137-69886376 | Rare:28 | ||||
chr14:73462188-73462497 | Common:1; Rare:50 |