Variant report

Variant	rs9396082
Chromosome Location	chr6:55215868-55215869
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1007968	0.95[CHB][hapmap];0.95[CHD][hapmap];0.89[JPT][hapmap]
rs10456708	0.85[JPT][hapmap]
rs10456709	0.81[JPT][hapmap]
rs13191759	0.94[ASN][1000 genomes]
rs13203638	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs3963	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap];0.80[MEX][hapmap]
rs4715529	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs4715530	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs6900362	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs6900899	0.81[JPT][hapmap]
rs6917737	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7452656	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap]
rs7743404	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7756270	0.95[CHB][hapmap];0.93[JPT][hapmap]
rs7757288	0.95[ASN][1000 genomes]
rs7757498	0.94[ASN][1000 genomes]
rs7775056	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs870806	0.84[MEX][hapmap]
rs905275	0.81[JPT][hapmap]
rs9296780	0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[JPT][hapmap]
rs9349776	0.83[CEU][hapmap];0.94[CHB][hapmap];0.94[JPT][hapmap]
rs9357860	0.95[ASN][1000 genomes]
rs9370414	0.86[CHD][hapmap];0.81[JPT][hapmap]
rs9382486	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs9382487	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs973052	0.81[JPT][hapmap]
rs991736	0.92[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885903	chr6:55142337-55344782	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1015161	chr6:55149388-55225072	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv1029279	chr6:55152655-55222696	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
4	nsv1034005	chr6:55152655-55225072	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
5	nsv1034960	chr6:55152655-55243149	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
6	nsv462947	chr6:55156812-55226013	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
7	nsv603162	chr6:55156812-55226013	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
8	nsv885904	chr6:55156812-55344782	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	esv3347672	chr6:55205042-55224529	ZNF genes & repeats Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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