Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34677086-34677304 | Rare:54 | ||||
chr20:34955743-34955947 | Common:1; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
chr20:35556712-35557109 | Common:2; Rare:107 | ||||
chr20:35664874-35665005 | Common:1; Rare:37 | ||||
chr20:35699344-35699456 | Rare:34 | ||||
chr20:35742175-35742619 | Common:5; Rare:138 | ||||
chr20:36951645-36951942 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):4 | ||||
chr20:37178865-37179205 | Rare:101 | ||||
chr20:37289545-37289672 | Common:1; Rare:37 | ||||
chr20:37527827-37528161 | Common:3; Rare:117 | ||||
chr20:38033417-38033775 | Common:2; Rare:104 | ||||
chr20:38962162-38962382 | Common:1; Rare:93 | ||||
chr20:41340561-41340842 | Rare:71 | ||||
chr20:43457805-43457907 | Rare:45 | ||||
chr20:43590595-43590985 | Common:1; Rare:87 |