Variant report

Variant	rs16893331
Chromosome Location	chr8:91489115-91489116
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11985438	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11991096	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11991586	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16904658	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16904669	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6997579	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7000048	1.00[AMR][1000 genomes]
rs7815421	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7815915	0.89[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7822308	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7823964	0.89[YRI][hapmap];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	chr8:91480600-91491200	Weak transcription	Liver	Liver

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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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