Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:162497741-162497867 | Common:1; Rare:42 | ||||
chr1:163203060-163203246 | Common:1; Rare:37 | ||||
chr1:163321723-163322047 | Common:1; Rare:91 | ||||
chr1:165768757-165769012 | Common:2; Rare:102 | ||||
chr1:166839322-166839535 | Rare:63 | ||||
chr1:166975334-166975607 | Common:2; Rare:80 | ||||
chr1:167093895-167094187 | Common:2; Rare:61 | ||||
chr1:167935869-167936261 | Common:1; Rare:108 | ||||
chr1:167936559-167936738 | Rare:59 | ||||
chr1:167936829-167936987 | Rare:66 | ||||
chr1:168178872-168179176 | Common:1; Rare:97 | ||||
chr1:168225936-168226056 | Common:1; Rare:41 | ||||
chr1:169367788-169368230 | Common:3; Rare:81 | ||||
chr1:169485766-169486206 | Common:2; Rare:116; Clinvar:5; Clinvar (benign):4 | ||||
chr1:169794868-169795053 | Common:3; Rare:39 |