Variant report

Variant	rs16882469
Chromosome Location	chr8:34442144-34442145
allele	A/G
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]
rs10503963	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs16882394	0.91[ASN][1000 genomes]
rs16882472	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16882616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16882698	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4739575	0.83[ASN][1000 genomes]
rs4739576	0.83[ASN][1000 genomes]
rs4739577	0.88[ASN][1000 genomes]
rs4739578	0.91[ASN][1000 genomes]
rs4739579	0.91[ASN][1000 genomes]
rs4739588	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6997049	0.99[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34441400-34442400	Flanking Active TSS	Liver	Liver
2	chr8:34442000-34442400	Enhancers	Stomach Mucosa	stomach

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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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