Variant report

Variant	rs56662827
Chromosome Location	chr3:146329419-146329420
allele	A/G
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]
rs12486975	1.00[ASN][1000 genomes]
rs16858692	1.00[ASN][1000 genomes]
rs55761292	1.00[ASN][1000 genomes]
rs61435584	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73000426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73000439	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73000440	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73000444	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73000447	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73157001	1.00[ASN][1000 genomes]
rs73159104	1.00[ASN][1000 genomes]
rs73159118	1.00[ASN][1000 genomes]
rs73159142	1.00[ASN][1000 genomes]
rs73159157	1.00[ASN][1000 genomes]
rs73159160	1.00[ASN][1000 genomes]
rs73159165	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:146328800-146329600	Enhancers	Fetal Stomach	stomach
2	chr3:146329400-146329600	Enhancers	Small Intestine	intestine

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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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