Variant report
Variant | rs73589947 |
---|---|
Chromosome Location | chr16:80169292-80169293 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr16:80164328..80166827-chr16:80167258..80169658,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs12324941 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs12325020 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs16952402 | 0.81[AFR][1000 genomes] |
rs16952518 | 0.97[AFR][1000 genomes] |
rs16952519 | 0.89[AMR][1000 genomes] |
rs28645719 | 0.89[AMR][1000 genomes] |
rs4888078 | 0.94[AFR][1000 genomes] |
rs59612196 | 0.82[AFR][1000 genomes] |
rs73571919 | 0.89[AMR][1000 genomes] |
rs73571920 | 0.89[AMR][1000 genomes] |
rs73571931 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs73583891 | 0.82[AFR][1000 genomes] |
rs73583892 | 0.82[AFR][1000 genomes] |
rs73585965 | 0.82[AFR][1000 genomes] |
rs73587905 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs73589923 | 0.97[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs73589928 | 0.88[AFR][1000 genomes] |
rs73589930 | 0.97[AFR][1000 genomes] |
rs9941188 | 0.89[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv833298 | chr16:80122337-80314603 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv1055982 | chr16:80151604-80202923 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | esv3385525 | chr16:80168065-80170628 | Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr16:80168600-80169400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |