Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45340381-45340496 | Not yet | Common:1; Rare:31; Clinvar:1 | 70 | ||
chr1:45500046-45500351 | Not yet | Common:1; Rare:75; Clinvar:4; Clinvar (pathogenic):3 | 209 | ||
chr1:45521827-45522013 | Not yet | Common:1; Rare:75 | 116 | ||
chr1:45550689-45551110 | Not yet | Common:3; Rare:110 | 234 | ||
chr1:45566643-45566902 | Not yet | Common:3; Rare:64 | 206 | ||
chr1:45583931-45584218 | Not yet | Common:1; Rare:110 | 210 | ||
chr1:45686452-45686668 | Not yet | Rare:78 | 135 | ||
chr1:45687054-45687365 | Not yet | Common:1; Rare:84 | 183 | ||
chr1:45688049-45688239 | Not yet | Common:1; Rare:53 | 168 | ||
chr1:45750607-45750823 | Not yet | Rare:79 | 126 | ||
chr1:46133037-46133209 | Not yet | Common:1; Rare:41 | 118 | ||
chr1:46198358-46198534 | Not yet | Common:1; Rare:73; Clinvar:1 | 94 | ||
chr1:46303140-46303775 | Not yet | Common:3; Rare:189 | 288 | ||
chr1:46339962-46340196 | Not yet | Common:4; Rare:47 | 156 | ||
chr1:46340664-46340819 | Not yet | Common:3; Rare:39 | 149 |