Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161199020-161199304 | Rare:43 | ||||
chr1:161225768-161226069 | Common:10; Rare:44 | ||||
chr1:161314265-161314435 | Common:3; Rare:70; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749749-161749826 | Rare:31 | ||||
chr1:161750248-161750447 | Rare:42 | ||||
chr1:161766125-161766371 | Common:3; Rare:70 | ||||
chr1:162497756-162497867 | Common:1; Rare:41 | ||||
chr1:162561349-162561700 | Common:3; Rare:134 | ||||
chr1:163321723-163322112 | Common:1; Rare:103 | ||||
chr1:165698500-165698762 | Common:5; Rare:105 | ||||
chr1:165768772-165768933 | Common:1; Rare:71 | ||||
chr1:166839348-166839522 | Rare:51 | ||||
chr1:167935950-167936249 | Common:1; Rare:91 | ||||
chr1:168225714-168226056 | Common:3; Rare:111 | ||||
chr1:169367725-169368271 | Common:3; Rare:116 |