Variant report

Variant	rs61443691
Chromosome Location	chr11:74923607-74923608
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17133818	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17133831	0.88[ASN][1000 genomes]
rs17133844	0.88[ASN][1000 genomes]
rs17133848	0.88[ASN][1000 genomes]
rs1801906	0.87[ASN][1000 genomes]
rs2035208	0.88[ASN][1000 genomes]
rs3781726	0.95[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3781727	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs41298121	0.87[ASN][1000 genomes]
rs56253315	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56738638	0.88[ASN][1000 genomes]
rs57279023	0.88[ASN][1000 genomes]
rs58769063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73488760	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73488764	0.88[ASN][1000 genomes]
rs7924924	0.88[ASN][1000 genomes]
rs7951787	0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74922600-74923800	Enhancers	Pancreas	Pancrea

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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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