Variant report

Variant	rs11174361
Chromosome Location	chr12:62571029-62571030
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10784287	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10877804	0.95[CHB][hapmap]
rs10877817	0.82[ASN][1000 genomes]
rs11174358	1.00[CHB][hapmap]
rs11174360	1.00[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11174368	0.91[ASN][1000 genomes]
rs11174369	0.92[ASN][1000 genomes]
rs11174373	0.92[ASN][1000 genomes]
rs11174377	0.83[ASN][1000 genomes]
rs11174378	0.82[ASN][1000 genomes]
rs12823493	0.82[ASN][1000 genomes]
rs1406799	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1920087	0.82[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1920096	0.90[CHB][hapmap]
rs2884779	0.90[CHB][hapmap]
rs3759290	1.00[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs4143667	0.80[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7305206	0.82[CHB][hapmap]
rs7305482	0.81[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[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	nsv832435	chr12:62407000-62601835	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr12:62567600-62572400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr12:62568800-62581800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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