Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10099045	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10100459	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12375320	0.94[ASN][1000 genomes]
rs12546239	0.85[ASN][1000 genomes]
rs12547877	0.94[ASN][1000 genomes]
rs12678112	0.85[ASN][1000 genomes]
rs13264902	0.83[AFR][1000 genomes]
rs16882264	0.99[ASN][1000 genomes]
rs2028776	0.92[ASN][1000 genomes]
rs2044355	0.84[EUR][1000 genomes]
rs2166231	0.84[EUR][1000 genomes]
rs28503648	0.92[ASN][1000 genomes]
rs28521494	0.83[AFR][1000 genomes]
rs28545279	0.90[ASN][1000 genomes]
rs2896967	0.84[EUR][1000 genomes]
rs4739565	0.93[ASN][1000 genomes]
rs55752257	0.94[ASN][1000 genomes]
rs55849895	0.85[ASN][1000 genomes]
rs56355533	0.92[ASN][1000 genomes]
rs59516528	0.93[ASN][1000 genomes]
rs6468257	0.88[YRI][hapmap]
rs6468262	0.94[ASN][1000 genomes]
rs6993906	0.85[ASN][1000 genomes]
rs7012499	0.94[ASN][1000 genomes]
rs7464162	0.93[ASN][1000 genomes]
rs7815684	0.85[ASN][1000 genomes]
rs7823416	0.90[JPT][hapmap];0.88[YRI][hapmap]
rs7827467	0.94[ASN][1000 genomes]
rs7833514	0.84[EUR][1000 genomes]
rs7834257	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7836137	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9297220	0.84[EUR][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	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34325600-34327200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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