Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160343163-160343403 | Rare:95 | ||||
chr1:160400348-160400615 | Common:1; Rare:64 | ||||
chr1:161045860-161046099 | Common:1; Rare:67 | ||||
chr1:161117951-161118141 | Rare:92 | ||||
chr1:161118242-161118327 | Rare:19 | ||||
chr1:161132572-161132681 | Common:1; Rare:36 | ||||
chr1:161153733-161153792 | Rare:16 | ||||
chr1:161159392-161159555 | Common:1; Rare:51 | ||||
chr1:161166257-161166537 | Common:3; Rare:70; Clinvar:5; Clinvar (benign):1 | ||||
chr1:161197206-161197459 | Common:3; Rare:46 | ||||
chr1:161199014-161199326 | Rare:47 | ||||
chr1:161225797-161226069 | Common:9; Rare:39 | ||||
chr1:161258545-161258749 | Common:1; Rare:47 | ||||
chr1:161314260-161314412 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749623-161749850 | Rare:77 |