Variant report

Variant	rs3811755
Chromosome Location	chr4:118496919-118496920
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11098396	0.96[ASN][1000 genomes]
rs11562892	0.97[ASN][1000 genomes]
rs11733276	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11734303	0.82[ASN][1000 genomes]
rs1387528	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs17862040	0.91[ASN][1000 genomes]
rs17862950	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs17863861	1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[ASN][1000 genomes]
rs17863866	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17866159	0.81[ASN][1000 genomes]
rs17867500	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs17867501	1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs1948233	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2245104	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap]
rs2245110	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2245138	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2245142	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2245255	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2245313	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2245321	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2245354	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2635192	0.82[ASN][1000 genomes]
rs2635223	0.80[ASN][1000 genomes]
rs2635249	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2635360	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2635362	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2635363	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2635364	1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs3811753	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap]
rs6534043	0.83[ASN][1000 genomes]
rs923442	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs923443	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	nsv482430	chr4:118347180-118497181	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv879831	chr4:118470151-118502728	Flanking Active TSS Active TSS Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv966313	chr4:118495717-118496996	Inactive region	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3811755	QRFPR	cis	cerebellum	SCAN

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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