Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:3126784-3127021 | Common:4; Rare:104; Clinvar (benign):4 | ||||
chr3:3179679-3179807 | Common:1; Rare:48; Clinvar:1 | ||||
chr3:4303091-4303405 | Common:2; Rare:91 | ||||
chr3:4467226-4467313 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr3:4493177-4493348 | Rare:60 | ||||
chr3:4980390-4980591 | Common:1; Rare:55 | ||||
chr3:8501638-8501941 | Common:2; Rare:111 | ||||
chr3:9249627-9249743 | Common:1; Rare:34 | ||||
chr3:9362978-9363109 | Common:1; Rare:50 | ||||
chr3:9397437-9397706 | Common:1; Rare:98 | ||||
chr3:9397834-9397880 | Rare:6 | ||||
chr3:9749783-9749983 | Rare:64 | ||||
chr3:9792369-9792590 | Rare:62 | ||||
chr3:9792701-9793124 | Common:3; Rare:149 | ||||
chr3:9843986-9844134 | Common:2; Rare:55 |