Variant report

Variant	rs9320629
Chromosome Location	chr6:118352476-118352477
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs11153713	0.85[CEU][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes]
rs11153717	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11153718	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12190596	0.94[CEU][hapmap];0.86[JPT][hapmap]
rs12191412	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12192479	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12206104	0.84[CEU][hapmap]
rs12207545	0.93[CEU][hapmap]
rs12208433	0.82[CEU][hapmap]
rs12213057	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs12213071	0.85[CEU][hapmap]
rs1547754	0.90[CEU][hapmap];0.82[JPT][hapmap];0.86[EUR][1000 genomes]
rs35943167	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4132664	0.95[CEU][hapmap];0.83[CHB][hapmap];0.93[JPT][hapmap];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4245492	0.95[CEU][hapmap];0.88[JPT][hapmap];0.95[EUR][1000 genomes]
rs4283912	0.85[CEU][hapmap]
rs4373391	0.95[CEU][hapmap];0.82[JPT][hapmap];0.98[EUR][1000 genomes]
rs4479971	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4945607	0.91[EUR][1000 genomes]
rs4945608	0.97[EUR][1000 genomes]
rs6900812	0.95[EUR][1000 genomes]
rs7738379	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9320626	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9320627	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9320628	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9320630	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9320634	0.90[CEU][hapmap];0.87[JPT][hapmap]
rs9320635	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9320636	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9320637	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9372494	0.87[JPT][hapmap];0.83[AMR][1000 genomes]
rs9374700	0.95[CEU][hapmap];0.83[JPT][hapmap];0.94[EUR][1000 genomes]
rs9374704	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9374708	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9374709	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9374711	0.88[CEU][hapmap]
rs9387537	0.83[EUR][1000 genomes]
rs9387539	0.99[EUR][1000 genomes]
rs9387547	0.88[CEU][hapmap];0.90[JPT][hapmap]
rs9387550	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9398474	0.91[CEU][hapmap];0.83[JPT][hapmap];0.92[EUR][1000 genomes]
rs9398476	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs9398477	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9401047	0.91[CEU][hapmap];0.83[JPT][hapmap];0.92[EUR][1000 genomes]
rs9401049	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9401050	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9401051	0.88[CEU][hapmap];0.87[JPT][hapmap]
rs9401052	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9401053	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118343400-118354800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr6:118351600-118352600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:118352200-118353400	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain

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