Variant report

Variant	rs11174364
Chromosome Location	chr12:62580013-62580014
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10784286	0.83[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs11174365	0.89[MKK][hapmap]
rs1245637	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1245639	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs1245643	0.86[ASN][1000 genomes]
rs1245646	0.86[ASN][1000 genomes]
rs1245649	0.86[ASN][1000 genomes]
rs1245650	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1245661	0.86[ASN][1000 genomes]
rs1920085	0.86[ASN][1000 genomes]
rs1920086	0.81[CHD][hapmap];0.90[JPT][hapmap];0.89[ASN][1000 genomes]
rs2700270	0.86[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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11174364	MARS	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62568800-62581800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr12:62578600-62581800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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