Variant report

Variant	rs11564282
Chromosome Location	chr12:40378739-40378740
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10506145	1.00[JPT][hapmap]
rs1086490	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10877837	0.83[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs11174370	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs11174427	0.83[CEU][hapmap];0.85[EUR][1000 genomes]
rs11174533	0.82[EUR][1000 genomes]
rs11564133	1.00[JPT][hapmap]
rs11564139	1.00[JPT][hapmap]
rs11564160	1.00[JPT][hapmap]
rs11564194	1.00[JPT][hapmap]
rs11564221	0.81[CEU][hapmap];0.87[EUR][1000 genomes]
rs11564223	1.00[JPT][hapmap]
rs12312535	1.00[JPT][hapmap]
rs12371119	0.80[CEU][hapmap];1.00[JPT][hapmap]
rs12810368	1.00[JPT][hapmap]
rs12827948	1.00[JPT][hapmap]
rs1482282	1.00[JPT][hapmap]
rs17442304	1.00[JPT][hapmap]
rs17442469	1.00[JPT][hapmap]
rs17442756	1.00[JPT][hapmap]
rs17443112	1.00[JPT][hapmap]
rs17483628	1.00[JPT][hapmap]
rs17489611	0.81[YRI][hapmap]
rs17518476	0.81[YRI][hapmap]
rs17559478	1.00[JPT][hapmap]
rs2046929	1.00[JPT][hapmap]
rs2404574	1.00[JPT][hapmap]
rs2708404	1.00[JPT][hapmap]
rs28370607	0.83[CEU][hapmap];0.85[EUR][1000 genomes]
rs28370611	0.85[EUR][1000 genomes]
rs28370644	1.00[JPT][hapmap]
rs28370656	1.00[JPT][hapmap]
rs28370659	1.00[JPT][hapmap]
rs28370728	0.80[YRI][hapmap]
rs4399379	1.00[JPT][hapmap]
rs7306718	1.00[JPT][hapmap]
rs73280629	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7484475	1.00[JPT][hapmap]
rs7969495	1.00[JPT][hapmap]
rs7974522	1.00[JPT][hapmap]
rs7974972	1.00[JPT][hapmap]
rs992851	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046428	chr12:40226283-40439843	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv541481	chr12:40226283-40439843	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
3	nsv1052202	chr12:40322607-40406760	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region miRNA target site	4 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	chr12:40364400-40391400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr12:40366400-40390200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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