Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167936544-167936987 | Common:1; Rare:160 | ||||
chr1:169367740-169368256 | Common:3; Rare:106 | ||||
chr1:169485691-169486194 | Common:1; Rare:151; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794690-169795053 | Common:3; Rare:66 | ||||
chr1:170074464-170074542 | Common:1; Rare:36 | ||||
chr1:170074557-170074771 | Common:2; Rare:54 | ||||
chr1:170531854-170532191 | Common:3; Rare:94; Clinvar:1 | ||||
chr1:170663031-170663197 | Rare:42 | ||||
chr1:171485404-171485598 | Rare:77 | ||||
chr1:171652227-171652371 | Rare:50; Clinvar:4 | ||||
chr1:171652433-171652784 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:171741925-171742218 | Common:2; Rare:96 | ||||
chr1:171781510-171781718 | Common:2; Rare:52 | ||||
chr1:171841381-171841580 | Common:2; Rare:61 | ||||
chr1:173476883-173477492 | Common:7; Rare:189 |