Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161223625-161223734 | Rare:20 | ||||
chr1:161225714-161226084 | Common:10; Rare:54 | ||||
chr1:161314262-161314425 | Common:3; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161367855-161367897 | Rare:10 | ||||
chr1:161750264-161750489 | Rare:37 | ||||
chr1:161766147-161766371 | Common:3; Rare:66 | ||||
chr1:162023636-162023945 | Common:1; Rare:85 | ||||
chr1:162497720-162497867 | Common:2; Rare:48 | ||||
chr1:162561346-162561700 | Common:3; Rare:134 | ||||
chr1:162631662-162631981 | Rare:58 | ||||
chr1:162790451-162790793 | Common:4; Rare:90 | ||||
chr1:163202790-163203251 | Common:1; Rare:91 | ||||
chr1:163321723-163322057 | Common:1; Rare:91 | ||||
chr1:164559596-164559854 | Common:3; Rare:61 | ||||
chr1:165630811-165630867 | Rare:18 |