Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20684467-20684619 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr14:20989733-20990014 | Common:6; Rare:63 | ||||
chr14:21476909-21477261 | Common:1; Rare:101 | ||||
chr14:22766508-22766717 | Common:1; Rare:109 | ||||
chr14:23321785-23322017 | Common:2; Rare:61 | ||||
chr14:23953658-23953849 | Common:7; Rare:74 | ||||
chr14:24114938-24115291 | Common:2; Rare:102 | ||||
chr14:24146574-24146751 | Rare:59 | ||||
chr14:24195414-24195769 | Common:1; Rare:83 | ||||
chr14:24232317-24232721 | Common:8; Rare:94 | ||||
chr14:24232820-24232939 | Common:1; Rare:25 | ||||
chr14:24271482-24271642 | Common:1; Rare:43 | ||||
chr14:24299712-24299922 | Common:5; Rare:72 | ||||
chr14:24429855-24429994 | Common:1; Rare:33 | ||||
chr14:24442702-24443010 | Common:5; Rare:100 |