Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20684447-20684595 | Common:1; Rare:24; Clinvar (benign):1 | ||||
chr14:21383917-21384284 | Common:8; Rare:121 | ||||
chr14:21456041-21456134 | Common:2; Rare:23 | ||||
chr14:21476878-21477267 | Common:2; Rare:124 | ||||
chr14:21511216-21511557 | Rare:103 | ||||
chr14:22588964-22589017 | Rare:7 | ||||
chr14:22589144-22589463 | Common:4; Rare:103 | ||||
chr14:22766524-22766710 | Common:1; Rare:94 | ||||
chr14:22829781-22829983 | Common:1; Rare:77 | ||||
chr14:22836836-22836875 | Common:1; Rare:11 | ||||
chr14:22871651-22871968 | Rare:80 | ||||
chr14:22872091-22872222 | Common:2; Rare:29 | ||||
chr14:22919090-22919486 | Common:8; Rare:111 | ||||
chr14:22929341-22929609 | Rare:66 | ||||
chr14:22956995-22957185 | Rare:55 |