Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35353941-35354069 | Common:2; Rare:14 | ||||
chr14:49633866-49634064 | Common:1; Rare:72; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr14:49862619-49863036 | Common:1; Rare:187 | ||||
chr14:50000000-50000287 | Common:2; Rare:44 | ||||
chr14:50001221-50001395 | Common:2; Rare:37 | ||||
chr14:53850796-53850994 | Common:1; Rare:33 | ||||
chr14:54837832-54838081 | Common:2; Rare:35 | ||||
chr14:58260871-58261019 | Rare:39 | ||||
chr14:60149388-60149733 | Common:2; Rare:90 | ||||
chr14:61720110-61720421 | Common:1; Rare:62 | ||||
chr14:61746736-61746965 | Common:1; Rare:37 | ||||
chr14:61751064-61751207 | Rare:36 | ||||
chr14:64112916-64113135 | Rare:38 | ||||
chr14:64438853-64439157 | Rare:51 | ||||
chr14:64444596-64444731 | Rare:38 |