Variant report
Variant | rs59437380 |
---|---|
Chromosome Location | chr1:159217348-159217349 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10047107 | 1.00[EUR][1000 genomes] |
rs10437336 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10437337 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs10489847 | 1.00[EUR][1000 genomes] |
rs10489850 | 1.00[EUR][1000 genomes] |
rs10489851 | 1.00[EUR][1000 genomes] |
rs10489852 | 1.00[EUR][1000 genomes] |
rs10489853 | 1.00[EUR][1000 genomes] |
rs11265145 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11265147 | 0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11265148 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11265151 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11265153 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs11265167 | 1.00[EUR][1000 genomes] |
rs12057331 | 1.00[EUR][1000 genomes] |
rs12060241 | 1.00[EUR][1000 genomes] |
rs12062367 | 1.00[EUR][1000 genomes] |
rs12063682 | 1.00[EUR][1000 genomes] |
rs12063973 | 1.00[EUR][1000 genomes] |
rs12064129 | 1.00[EUR][1000 genomes] |
rs12064962 | 1.00[EUR][1000 genomes] |
rs12067678 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12068030 | 1.00[EUR][1000 genomes] |
rs12068651 | 0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12074418 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12074452 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12074934 | 1.00[EUR][1000 genomes] |
rs12078114 | 1.00[EUR][1000 genomes] |
rs12078168 | 1.00[EUR][1000 genomes] |
rs12079229 | 1.00[EUR][1000 genomes] |
rs12079235 | 1.00[EUR][1000 genomes] |
rs12082893 | 1.00[EUR][1000 genomes] |
rs12085001 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs12085085 | 1.00[EUR][1000 genomes] |
rs12085686 | 1.00[EUR][1000 genomes] |
rs12086637 | 1.00[EUR][1000 genomes] |
rs12086871 | 1.00[EUR][1000 genomes] |
rs12087366 | 1.00[EUR][1000 genomes] |
rs12095599 | 1.00[EUR][1000 genomes] |
rs12096257 | 1.00[EUR][1000 genomes] |
rs13374880 | 1.00[EUR][1000 genomes] |
rs16841729 | 1.00[EUR][1000 genomes] |
rs16841784 | 1.00[EUR][1000 genomes] |
rs16841789 | 1.00[EUR][1000 genomes] |
rs16841937 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs16841970 | 1.00[EUR][1000 genomes] |
rs16842041 | 1.00[EUR][1000 genomes] |
rs2325923 | 1.00[EUR][1000 genomes] |
rs2325925 | 1.00[EUR][1000 genomes] |
rs2325927 | 1.00[EUR][1000 genomes] |
rs2746042 | 1.00[EUR][1000 genomes] |
rs28537540 | 1.00[EUR][1000 genomes] |
rs3026944 | 1.00[EUR][1000 genomes] |
rs3026947 | 1.00[EUR][1000 genomes] |
rs3026970 | 1.00[EUR][1000 genomes] |
rs3026984 | 1.00[EUR][1000 genomes] |
rs3027040 | 1.00[EUR][1000 genomes] |
rs3027041 | 0.85[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3027046 | 1.00[EUR][1000 genomes] |
rs3027047 | 1.00[EUR][1000 genomes] |
rs3027050 | 1.00[EUR][1000 genomes] |
rs3027057 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs3027066 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs34152791 | 0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs34870435 | 1.00[EUR][1000 genomes] |
rs35122728 | 1.00[EUR][1000 genomes] |
rs35507685 | 0.81[AFR][1000 genomes] |
rs36103299 | 1.00[EUR][1000 genomes] |
rs36160848 | 1.00[EUR][1000 genomes] |
rs3893415 | 1.00[EUR][1000 genomes] |
rs4255380 | 1.00[EUR][1000 genomes] |
rs4534374 | 1.00[EUR][1000 genomes] |
rs4568831 | 1.00[EUR][1000 genomes] |
rs56113018 | 0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6656586 | 1.00[EUR][1000 genomes] |
rs6670082 | 1.00[EUR][1000 genomes] |
rs6670592 | 1.00[EUR][1000 genomes] |
rs6670703 | 1.00[EUR][1000 genomes] |
rs6673514 | 1.00[EUR][1000 genomes] |
rs6695631 | 1.00[EUR][1000 genomes] |
rs6696230 | 1.00[EUR][1000 genomes] |
rs73023773 | 1.00[EUR][1000 genomes] |
rs73023775 | 1.00[EUR][1000 genomes] |
rs73027932 | 1.00[EUR][1000 genomes] |
rs74122265 | 1.00[EUR][1000 genomes] |
rs7515532 | 1.00[EUR][1000 genomes] |
rs7552141 | 1.00[EUR][1000 genomes] |
rs7556244 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv872487 | chr1:159196765-159342439 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:159216600-159217400 | Enhancers | HMEC | breast |
2 | chr1:159217000-159218400 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr1:159217000-159218400 | Enhancers | NHEK | skin |
4 | chr1:159217200-159218400 | Weak transcription | Esophagus | oesophagus |