Variant report

Variant	rs11013266
Chromosome Location	chr10:23328338-23328339
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12240971	1.00[AMR][1000 genomes]
rs12243018	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12243747	0.83[AFR][1000 genomes]
rs12249351	1.00[AMR][1000 genomes]
rs12251949	1.00[AMR][1000 genomes]
rs12260464	0.89[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12261689	0.83[YRI][hapmap];1.00[AMR][1000 genomes]
rs12262236	0.88[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12269303	0.92[AFR][1000 genomes]
rs7072923	1.00[AMR][1000 genomes]
rs7097832	1.00[AMR][1000 genomes]
rs9971201	1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23328000-23331200	Weak transcription	K562	blood

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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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