Variant report

Variant	rs4755319
Chromosome Location	chr11:45381346-45381347
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10838456	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11038408	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11038412	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11607009	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4755318	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4755320	0.93[ASW][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];0.90[LWK][hapmap];0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4755321	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4755978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61880359	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61882561	1.00[ASN][1000 genomes]
rs61882562	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61882563	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61882564	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61882566	0.80[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs61882568	1.00[ASN][1000 genomes]
rs7943277	1.00[ASN][1000 genomes]
rs7943376	1.00[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	nsv530619	chr11:45294176-45553928	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4755319	OR4X2	cis	parietal	SCAN

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45378000-45387800	Weak transcription	Lung	lung
2	chr11:45378200-45387200	Weak transcription	Brain Anterior Caudate	brain
3	chr11:45378200-45387800	Weak transcription	Fetal Brain Male	brain

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Input of quick search could be:

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

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