Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367713-169368265 | Common:3; Rare:120 | ||||
chr1:169427350-169427654 | Common:2; Rare:65 | ||||
chr1:169485682-169486264 | Common:2; Rare:164; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169586198-169586598 | Common:4; Rare:161; Clinvar:5; Clinvar (benign):2 | ||||
chr1:169794586-169795108 | Common:5; Rare:115 | ||||
chr1:169795110-169796057 | Common:12; Rare:257 | ||||
chr1:169893589-169893745 | Common:3; Rare:54 | ||||
chr1:169893871-169894029 | Common:2; Rare:49 | ||||
chr1:169894230-169894408 | Common:3; Rare:56 | ||||
chr1:170074566-170074778 | Common:2; Rare:52 | ||||
chr1:170531754-170532179 | Common:3; Rare:117; Clinvar:1 | ||||
chr1:171485328-171485597 | Rare:98 | ||||
chr1:171741909-171742164 | Common:2; Rare:82 | ||||
chr1:171781156-171781726 | Common:5; Rare:149 | ||||
chr1:171841344-171841542 | Common:2; Rare:62 |