Variant report

Variant	rs72967588
Chromosome Location	chr3:118119932-118119933
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs16828357	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55790104	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59536608	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72952707	1.00[EUR][1000 genomes]
rs72967585	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72967595	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72969510	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72969513	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:118119000-118120600	Enhancers	Liver	Liver
2	chr3:118119800-118120000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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