Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10956606	0.87[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs11991337	0.86[ASN][1000 genomes]
rs11996534	0.92[ASN][1000 genomes]
rs12541215	0.92[ASN][1000 genomes]
rs12542044	0.92[ASN][1000 genomes]
rs12543683	0.85[ASN][1000 genomes]
rs12543750	0.89[ASN][1000 genomes]
rs4422814	0.94[ASN][1000 genomes]
rs4551412	0.94[ASN][1000 genomes]
rs4560835	0.94[ASN][1000 genomes]
rs57808255	0.89[ASN][1000 genomes]
rs59229746	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6984328	0.92[ASN][1000 genomes]
rs7003176	0.91[ASN][1000 genomes]
rs7004083	0.90[ASN][1000 genomes]
rs73312729	0.93[ASN][1000 genomes]
rs73312731	0.92[ASN][1000 genomes]
rs73312758	0.94[ASN][1000 genomes]
rs73312787	0.86[ASN][1000 genomes]
rs7825634	1.00[ASN][1000 genomes]
rs7830901	0.91[ASN][1000 genomes]
rs7840137	0.86[AMR][1000 genomes];0.96[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	nsv1018991	chr8:91336887-91374274	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91352000-91364400	Weak transcription	K562	blood
2	chr8:91353200-91353400	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell

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