Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75069241-75069732 | Common:2; Rare:134 | ||||
chr14:75126973-75127120 | Rare:55 | ||||
chr14:75175957-75176234 | Common:2; Rare:48 | ||||
chr14:75176544-75176797 | Common:1; Rare:77 | ||||
chr14:75427643-75427768 | Rare:31 | ||||
chr14:75578309-75578706 | Common:2; Rare:81; Clinvar (benign):1 | ||||
chr14:75579503-75579608 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
chr14:75660819-75660992 | Rare:42 | ||||
chr14:75661084-75661304 | Common:3; Rare:49 | ||||
chr14:77320832-77321110 | Rare:88; Clinvar:1 | ||||
chr14:77377045-77377410 | Common:2; Rare:107 | ||||
chr14:77457550-77457844 | Common:1; Rare:92 | ||||
chr14:77457995-77458215 | Rare:55 | ||||
chr14:77707991-77708206 | Common:2; Rare:108 | ||||
chr14:77761123-77761262 | Rare:52 |