Variant report

Variant	rs12264620
Chromosome Location	chr10:44281425-44281426
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11238706	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12240973	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12249062	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12253404	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12268749	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57113623	0.87[EUR][1000 genomes]
rs60454219	1.00[EUR][1000 genomes]
rs60924513	0.87[EUR][1000 genomes]
rs61432090	1.00[EUR][1000 genomes]
rs61581987	1.00[EUR][1000 genomes]
rs73265875	1.00[EUR][1000 genomes]
rs73268482	1.00[EUR][1000 genomes]
rs73270326	1.00[EUR][1000 genomes]
rs73270329	1.00[EUR][1000 genomes]
rs73270364	1.00[EUR][1000 genomes]
rs73276542	0.87[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44277800-44295000	Weak transcription	Spleen	Spleen
2	chr10:44281400-44281600	Enhancers	Right Atrium	heart

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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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