Variant report

Variant	rs10282933
Chromosome Location	chr8:51155698-51155699
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10086021	0.87[AMR][1000 genomes]
rs10103929	0.87[AMR][1000 genomes]
rs10107397	0.90[CHD][hapmap];0.91[MEX][hapmap]
rs10504101	1.00[ASW][hapmap];0.94[CHD][hapmap];0.88[JPT][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];0.81[MKK][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10957899	0.88[JPT][hapmap]
rs11993995	0.90[AMR][1000 genomes]
rs11998724	0.87[AMR][1000 genomes]
rs1450123	0.86[ASW][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap];0.80[MEX][hapmap];0.90[YRI][hapmap];0.84[AMR][1000 genomes]
rs16914299	0.88[JPT][hapmap]
rs16914526	0.83[CHD][hapmap];0.88[JPT][hapmap]
rs16914623	0.81[CHB][hapmap];0.88[JPT][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs16914661	0.87[AMR][1000 genomes]
rs16914702	0.81[CHB][hapmap];0.88[JPT][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs16914726	0.89[CHD][hapmap];0.88[JPT][hapmap];0.80[MEX][hapmap];0.84[AMR][1000 genomes]
rs16914778	0.88[JPT][hapmap];0.90[AMR][1000 genomes]
rs2169183	0.81[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.90[MEX][hapmap];0.80[MKK][hapmap];0.90[YRI][hapmap]
rs28496647	0.84[AMR][1000 genomes]
rs28513173	0.84[AMR][1000 genomes]
rs28869785	0.87[AMR][1000 genomes]
rs28886897	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs28895348	0.87[AMR][1000 genomes]
rs4242461	0.86[ASW][hapmap];0.89[CHD][hapmap];0.88[JPT][hapmap]
rs4349993	0.88[JPT][hapmap]
rs4367560	0.88[JPT][hapmap]
rs4367564	0.89[CHD][hapmap];0.88[JPT][hapmap]
rs4376507	0.88[JPT][hapmap]
rs4416833	0.88[JPT][hapmap]
rs4449807	0.88[JPT][hapmap]
rs4523268	0.88[JPT][hapmap]
rs4524809	0.86[ASW][hapmap];0.88[JPT][hapmap]
rs4570174	0.88[JPT][hapmap]
rs4607635	0.88[JPT][hapmap]
rs4873441	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4873445	0.88[JPT][hapmap];1.00[YRI][hapmap]
rs4873450	1.00[ASW][hapmap];0.81[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];0.90[YRI][hapmap];0.80[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs4873455	0.89[CHD][hapmap];0.88[JPT][hapmap]
rs57368926	0.87[AMR][1000 genomes]
rs57879337	0.87[AMR][1000 genomes]
rs59878004	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6984454	0.88[JPT][hapmap]
rs73676273	0.81[AMR][1000 genomes]
rs73678730	0.87[AMR][1000 genomes]
rs73678735	0.87[AMR][1000 genomes]
rs73678750	0.84[AMR][1000 genomes]
rs7823310	0.88[JPT][hapmap]
rs921330	0.91[YRI][hapmap];0.90[AMR][1000 genomes]
rs9298318	0.89[CHD][hapmap];0.88[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916392	chr8:50827638-51395140	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	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

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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