Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343129-160343405 | Rare:102 | ||||
chr1:161021115-161021309 | Rare:53 | ||||
chr1:161038903-161039003 | Rare:40 | ||||
chr1:161045866-161046071 | Common:1; Rare:52 | ||||
chr1:161098182-161098388 | Common:1; Rare:31 | ||||
chr1:161117892-161118141 | Rare:109 | ||||
chr1:161118200-161118348 | Common:1; Rare:41 | ||||
chr1:161132411-161132708 | Common:1; Rare:95 | ||||
chr1:161153720-161153836 | Rare:29 | ||||
chr1:161159392-161159550 | Common:1; Rare:50 | ||||
chr1:161166255-161166544 | Common:3; Rare:74; Clinvar:5; Clinvar (benign):1 | ||||
chr1:161225697-161226079 | Common:10; Rare:54 | ||||
chr1:161307392-161307571 | Rare:44; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:161314305-161314423 | Common:2; Rare:55; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749638-161749915 | Rare:98 |