Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161117970-161118153 | Rare:99 | ||||
chr1:161132417-161132709 | Common:1; Rare:95 | ||||
chr1:161153739-161153792 | Rare:15 | ||||
chr1:161159392-161159520 | Common:1; Rare:34 | ||||
chr1:161197167-161197428 | Common:3; Rare:42 | ||||
chr1:161199053-161199299 | Rare:39 | ||||
chr1:161225768-161226069 | Common:10; Rare:44 | ||||
chr1:161314262-161314414 | Common:3; Rare:57; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749763-161749862 | Rare:44 | ||||
chr1:161750220-161750422 | Rare:51 | ||||
chr1:161766133-161766376 | Common:3; Rare:72 | ||||
chr1:162497741-162497859 | Common:1; Rare:35 | ||||
chr1:162561346-162561700 | Common:3; Rare:134 | ||||
chr1:162790516-162790774 | Common:3; Rare:72 | ||||
chr1:163321727-163322057 | Common:1; Rare:91 |