Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:2840629-2840765 | Common:1; Rare:53 | ||||
chr20:3209446-3209549 | Rare:36 | ||||
chr20:3767704-3768067 | Common:5; Rare:115 | ||||
chr20:3796334-3796548 | Common:3; Rare:45 | ||||
chr20:3820481-3820592 | Rare:42 | ||||
chr20:3846727-3846893 | Rare:49 | ||||
chr20:3889072-3889379 | Common:1; Rare:166; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr20:3889737-3889852 | Common:6; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr20:5119894-5120215 | Common:1; Rare:112 | ||||
chr20:5126530-5126814 | Common:3; Rare:79 | ||||
chr20:6005819-6006128 | Common:2; Rare:83 | ||||
chr20:13784894-13785103 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):3 | ||||
chr20:16573321-16573492 | Common:1; Rare:45 | ||||
chr20:17968417-17969118 | Common:9; Rare:273 | ||||
chr20:20017238-20017394 | Rare:56 |