Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24389354-24389509 | Rare:31 | ||||
chr14:31876888-31877014 | Rare:24 | ||||
chr14:32203267-32203571 | Common:12; Rare:128 | ||||
chr14:32627582-32627791 | Rare:29 | ||||
chr14:48456155-48456422 | Common:6; Rare:45 | ||||
chr14:49633930-49634070 | Common:1; Rare:57; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr14:49862708-49863020 | Rare:141 | ||||
chr14:61229552-61229648 | Rare:18 | ||||
chr14:61547248-61547407 | Rare:30 | ||||
chr14:68192185-68192303 | Rare:13 | ||||
chr14:68552578-68552883 | Common:2; Rare:46 | ||||
chr14:68563443-68563719 | Rare:51 | ||||
chr14:68593940-68594279 | Common:1; Rare:51 | ||||
chr14:68596763-68596843 | Common:2; Rare:12 | ||||
chr14:68795244-68795431 | Common:3; Rare:41 |