Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:50944399-50944603 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51240008-51240325 | Common:2; Rare:116 | ||||
chr14:51651438-51651462 | Rare:10 | ||||
chr14:51651620-51651984 | Common:4; Rare:102 | ||||
chr14:51860585-51860769 | Rare:53 | ||||
chr14:52068990-52069247 | Common:2; Rare:62 | ||||
chr14:52314112-52314369 | Common:1; Rare:70 | ||||
chr14:52552486-52552863 | Common:1; Rare:112 | ||||
chr14:52695496-52695809 | Common:1; Rare:85 | ||||
chr14:52791437-52791916 | Common:3; Rare:150 | ||||
chr14:52951003-52951429 | Common:4; Rare:150 | ||||
chr14:53152378-53152529 | Rare:56; Clinvar (benign):1 | ||||
chr14:53953371-53953645 | Common:2; Rare:80 | ||||
chr14:53956757-53957008 | Rare:57; Clinvar:1 | ||||
chr14:54567035-54567186 | Rare:41 |