Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:2971539-2971743 | Common:1; Rare:59 | ||||
chr6:2999675-3000019 | Common:10; Rare:66 | ||||
chr6:3118366-3118755 | Common:5; Rare:129 | ||||
chr6:3157521-3157648 | Common:6; Rare:48 | ||||
chr6:3231730-3231793 | Rare:8 | ||||
chr6:4021187-4021445 | Rare:113 | ||||
chr6:5260736-5261017 | Common:2; Rare:89; Clinvar (benign):2 | ||||
chr6:7108588-7108674 | Rare:29 | ||||
chr6:7313055-7313236 | Common:4; Rare:77 | ||||
chr6:7389684-7389875 | Common:2; Rare:66 | ||||
chr6:7541390-7541690 | Rare:91; Clinvar (benign):1 | ||||
chr6:7541840-7542084 | Common:3; Rare:100; Clinvar:15; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr6:8064338-8064576 | Common:4; Rare:71 | ||||
chr6:8102518-8102712 | Common:1; Rare:64 | ||||
chr6:8435485-8435659 | Common:3; Rare:69 |