Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:162023309-162023393 | Rare:28; Clinvar (pathogenic):1 | ||||
chr1:162023611-162023958 | Common:1; Rare:100 | ||||
chr1:162790447-162790765 | Common:3; Rare:79 | ||||
chr1:163202908-163203066 | Rare:29 | ||||
chr1:163321752-163322057 | Common:1; Rare:81 | ||||
chr1:165768777-165768933 | Common:1; Rare:69 | ||||
chr1:166839322-166839522 | Rare:57 | ||||
chr1:167935943-167936327 | Common:2; Rare:116 | ||||
chr1:167936544-167936994 | Common:1; Rare:163 | ||||
chr1:168225714-168226091 | Common:4; Rare:126 | ||||
chr1:169367773-169368250 | Common:3; Rare:91 | ||||
chr1:169485941-169486139 | Rare:48; Clinvar:1 | ||||
chr1:169794889-169795094 | Common:3; Rare:53 | ||||
chr1:170532074-170532210 | Rare:76; Clinvar:1 | ||||
chr1:170663031-170663209 | Rare:48 |