Variant report
Variant | rs4856645 |
---|---|
Chromosome Location | chr3:161374624-161374625 |
allele | G/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 | chr3:161373878..161376279-chr3:161388444..161390253,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs2063835 | 0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4269094 | 0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4389491 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4856708 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs62279587 | 0.82[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs62281367 | 0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs73166070 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs73166073 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7632851 | 0.89[ASN][1000 genomes] |
rs869772 | 0.89[ASN][1000 genomes] |
rs9812690 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9815734 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9824937 | 0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9837035 | 0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9867861 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9877005 | 0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs9881986 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv533237 | chr3:161019834-161804660 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 91 gene(s) | inside rSNPs | diseases |
2 | nsv829774 | chr3:161229405-161386919 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | esv2422309 | chr3:161242389-161425932 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | nsv877711 | chr3:161275848-161486665 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1004255 | chr3:161340249-161476537 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:161374400-161374800 | Enhancers | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |