Variant report
Variant | rs9917445 |
---|---|
Chromosome Location | chr20:15521364-15521365 |
allele | C/T |
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 |
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No data |
rs_ID | r2[population] |
---|---|
rs11697525 | 0.86[CEU][hapmap] |
rs11697986 | 0.86[CEU][hapmap];0.85[EUR][1000 genomes] |
rs1345368 | 0.90[ASW][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.81[YRI][hapmap] |
rs1547972 | 1.00[JPT][hapmap] |
rs16995898 | 0.90[ASW][hapmap];0.88[CHB][hapmap];0.89[CHD][hapmap];0.83[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap] |
rs1816000 | 0.90[ASW][hapmap];0.94[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap] |
rs2058735 | 0.96[ASN][1000 genomes] |
rs6034213 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap] |
rs6043349 | 1.00[CEU][hapmap];0.88[CHB][hapmap];0.81[JPT][hapmap] |
rs6043350 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];0.89[TSI][hapmap];0.81[YRI][hapmap] |
rs6043351 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap] |
rs6105428 | 0.93[CEU][hapmap];0.88[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs6110655 | 0.88[CHB][hapmap];0.89[CHD][hapmap];0.83[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs6110663 | 0.93[CEU][hapmap] |
rs6110672 | 0.86[CEU][hapmap];0.88[TSI][hapmap];0.83[EUR][1000 genomes] |
rs6110677 | 0.86[CEU][hapmap];0.88[TSI][hapmap];0.89[EUR][1000 genomes] |
rs6135432 | 0.87[CHB][hapmap];0.92[JPT][hapmap];0.86[ASN][1000 genomes] |
rs66767980 | 0.93[ASN][1000 genomes] |
rs73098214 | 0.85[EUR][1000 genomes] |
rs73098216 | 0.83[EUR][1000 genomes] |
rs73100236 | 0.85[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page:
1
No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1062252 | chr20:14964258-15547739 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | nsv544206 | chr20:14964258-15547739 | Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
3 | nsv869328 | chr20:15325423-16213898 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
4 | esv2751909 | chr20:15489871-15656007 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1057672 | chr20:15512342-15527164 | Enhancers Weak transcription | n/a | n/a | inside rSNPs | diseases |
No data |