Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:114281495-114281846 | Common:4; Rare:203 | ||||
chr13:114281852-114282114 | Common:5; Rare:116 | ||||
chr13:114282145-114282478 | Common:4; Rare:99 | ||||
chr14:20333257-20333463 | Common:1; Rare:41 | ||||
chr14:20343178-20343661 | Common:12; Rare:284 | ||||
chr14:20413161-20413233 | Common:1; Rare:11 | ||||
chr14:20413413-20413537 | Common:3; Rare:36 | ||||
chr14:20454696-20455568 | Common:7; Rare:228 | ||||
chr14:20461367-20461744 | Common:3; Rare:115 | ||||
chr14:20683890-20684286 | Common:20; Rare:172; Clinvar:2; Clinvar (benign):3 | ||||
chr14:20684453-20684745 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr14:20802795-20803048 | Common:1; Rare:42 | ||||
chr14:20989665-20990043 | Common:7; Rare:94 | ||||
chr14:21020983-21021256 | Rare:77 | ||||
chr14:21022062-21022449 | Common:1; Rare:102 |