Variant report

Variant	rs1157348
Chromosome Location	chr8:51489731-51489732
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10087387	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10088424	0.86[JPT][hapmap]
rs10088550	0.86[JPT][hapmap]
rs10106921	0.86[JPT][hapmap]
rs10107280	1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10108554	1.00[JPT][hapmap]
rs10110737	1.00[JPT][hapmap]
rs11994238	0.86[JPT][hapmap]
rs12334955	1.00[JPT][hapmap]
rs12675489	1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12677318	0.84[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12679674	0.86[JPT][hapmap]
rs1384828	0.86[JPT][hapmap]
rs1384830	0.85[JPT][hapmap]
rs1481474	0.86[JPT][hapmap];0.86[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16915036	1.00[JPT][hapmap]
rs16915079	0.85[JPT][hapmap]
rs16915100	0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2016596	0.85[CHB][hapmap]
rs2046355	1.00[JPT][hapmap]
rs28412668	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs28435842	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs3849806	0.86[JPT][hapmap];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4873467	0.82[CHB][hapmap];0.86[JPT][hapmap];0.80[YRI][hapmap];0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6473239	1.00[JPT][hapmap]
rs6473247	1.00[JPT][hapmap]
rs6473249	1.00[JPT][hapmap]
rs6473253	0.85[JPT][hapmap]
rs6998737	0.85[JPT][hapmap]
rs7002065	0.86[JPT][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7017918	0.86[JPT][hapmap]
rs7842259	0.84[CHB][hapmap]
rs922723	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9298339	1.00[JPT][hapmap]
rs996167	0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948436	chr8:51115028-51917504	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv429914	chr8:51371447-51617647	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv531502	chr8:51390997-51703556	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv3514165	chr8:51416583-51923545	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	esv3514166	chr8:51416583-51923545	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv890873	chr8:51462163-51612641	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	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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