Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633835-49634092 | Common:1; Rare:96; Clinvar:12; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr14:49789497-49789682 | Rare:42 | ||||
chr14:49802669-49802920 | Rare:64 | ||||
chr14:49862619-49863044 | Common:1; Rare:191 | ||||
chr14:52315362-52315537 | Rare:41 | ||||
chr14:52881454-52881743 | Common:1; Rare:48 | ||||
chr14:55103185-55103491 | Common:1; Rare:67 | ||||
chr14:56310793-56310944 | Common:2; Rare:30 | ||||
chr14:58260734-58261019 | Common:1; Rare:71 | ||||
chr14:58266275-58266595 | Common:2; Rare:63 | ||||
chr14:58266766-58266919 | Rare:31 | ||||
chr14:58267305-58267498 | Rare:42 | ||||
chr14:59325429-59325670 | Common:1; Rare:41 | ||||
chr14:60156122-60156419 | Common:5; Rare:65 | ||||
chr14:61338190-61338428 | Common:2; Rare:38 |