Variant report

Variant	rs1362479
Chromosome Location	chr2:67167431-67167432
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11674518	0.82[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[ASN][1000 genomes]
rs11684557	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11690973	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11693667	1.00[ASN][1000 genomes]
rs1420367	1.00[ASN][1000 genomes]
rs1420368	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17032787	0.85[AFR][1000 genomes]
rs57130923	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6719096	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6732212	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7594373	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67165800-67179400	Weak transcription	Fetal Lung	lung
2	chr2:67166800-67169400	Enhancers	Fetal Kidney	kidney
3	chr2:67167000-67169400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr2:67167400-67167600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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