Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20694058-20694358 | Rare:49 | ||||
chr14:21060959-21061317 | Common:3; Rare:78 | ||||
chr14:24818222-24818389 | Rare:34 | ||||
chr14:32203267-32203616 | Common:13; Rare:146 | ||||
chr14:32572430-32572497 | Rare:9 | ||||
chr14:49622239-49622440 | Rare:42; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr14:49633861-49634043 | Common:1; Rare:69; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:49862284-49862559 | Common:1; Rare:63 | ||||
chr14:49862642-49863050 | Common:1; Rare:186 | ||||
chr14:50001250-50001379 | Common:2; Rare:25 | ||||
chr14:50003300-50003613 | Common:2; Rare:86 | ||||
chr14:53613935-53614091 | Rare:30 | ||||
chr14:56310771-56311021 | Common:2; Rare:43 | ||||
chr14:58266567-58266683 | Common:1; Rare:23 | ||||
chr14:61751067-61751194 | Rare:29 |