Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161363438-161363544 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
chr1:165851362-165851589 | Common:1; Rare:43 | ||||
chr1:165896724-165896972 | Common:1; Rare:47 | ||||
chr1:167745036-167745241 | Rare:29 | ||||
chr1:167772078-167772298 | Common:2; Rare:56 | ||||
chr1:167787779-167787820 | Rare:13 | ||||
chr1:167820284-167820360 | Rare:19 | ||||
chr1:167951640-167951862 | Common:1; Rare:38 | ||||
chr1:168031408-168031591 | Common:1; Rare:28 | ||||
chr1:169235137-169235335 | Rare:38 | ||||
chr1:169383570-169383880 | Common:3; Rare:46 | ||||
chr1:169467175-169467447 | Common:5; Rare:39 | ||||
chr1:170669239-170669308 | Rare:9 | ||||
chr1:170669476-170669509 | Rare:8 | ||||
chr1:170674369-170674651 | Rare:52 |