Variant report

Variant	rs11623063
Chromosome Location	chr14:63380533-63380534
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10134985	0.93[CEU][hapmap]
rs10483762	1.00[CEU][hapmap];0.82[TSI][hapmap];0.92[EUR][1000 genomes]
rs10873164	0.92[CEU][hapmap]
rs11158459	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11625796	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.85[TSI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11628836	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs11846438	0.82[CHB][hapmap]
rs12431704	0.93[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12588293	1.00[CEU][hapmap]
rs12881527	0.96[CEU][hapmap];0.83[TSI][hapmap];0.91[EUR][1000 genomes]
rs12881682	1.00[CEU][hapmap]
rs1950572	1.00[CEU][hapmap];0.83[TSI][hapmap]
rs1956024	1.00[CEU][hapmap]
rs1956027	0.85[CEU][hapmap];0.86[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs2144775	0.89[CEU][hapmap]
rs2356098	0.88[EUR][1000 genomes]
rs243155	0.82[CHB][hapmap]
rs243156	0.82[CHB][hapmap]
rs243157	0.82[CHB][hapmap]
rs4146434	1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs4146435	1.00[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs6573462	0.93[CEU][hapmap]
rs6573466	1.00[CEU][hapmap];0.82[TSI][hapmap]
rs6573467	1.00[CEU][hapmap];0.87[TSI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7155227	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7155469	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.87[TSI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7156354	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.87[TSI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8015097	0.93[CEU][hapmap]
rs8019236	1.00[CEU][hapmap]
rs9972116	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv1042953	chr14:63314591-63384260	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63380400-63381400	Enhancers	Muscle Satellite Cultured Cells	--

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