Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:114281353-114281660 | Common:5; Rare:126 | ||||
chr14:20343407-20343647 | Common:7; Rare:115 | ||||
chr14:20455051-20455315 | Common:2; Rare:78 | ||||
chr14:20460156-20460380 | Common:3; Rare:49 | ||||
chr14:20461728-20462016 | Common:3; Rare:68 | ||||
chr14:20684438-20684614 | Common:2; Rare:29; Clinvar (benign):2 | ||||
chr14:21211552-21211883 | Common:3; Rare:85 | ||||
chr14:21262900-21262985 | Rare:14 | ||||
chr14:21437228-21437396 | Common:3; Rare:73 | ||||
chr14:21476870-21477271 | Common:2; Rare:131 | ||||
chr14:22766554-22766741 | Common:1; Rare:107 | ||||
chr14:22776002-22776313 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:22815781-22816043 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr14:22829742-22829931 | Common:1; Rare:61 | ||||
chr14:22836575-22836675 | Rare:21 |