Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:28766545-28766768 | Common:2; Rare:70 | ||||
chr14:28768233-28768394 | Rare:38; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:28774497-28774801 | Common:3; Rare:56 | ||||
chr14:28775056-28775175 | Rare:23 | ||||
chr14:29274950-29275222 | Common:2; Rare:53 | ||||
chr14:29378418-29378454 | Rare:10 | ||||
chr14:29392019-29392060 | Rare:4 | ||||
chr14:32203242-32203616 | Common:13; Rare:164 | ||||
chr14:49633932-49634084 | Common:1; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49862642-49863012 | Common:1; Rare:172 | ||||
chr14:69886145-69886462 | Rare:35 | ||||
chr14:74764244-74764267 | Common:1; Rare:9 | ||||
chr14:81219339-81219502 | Rare:36 | ||||
chr14:90383208-90383531 | Common:2; Rare:111 | ||||
chr14:100825921-100826160 | Rare:47 |