Variant report

Variant	rs73672188
Chromosome Location	chr8:34147472-34147473
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16881980	0.81[EUR][1000 genomes]
rs16882130	0.81[EUR][1000 genomes]
rs28703850	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs55935531	0.81[EUR][1000 genomes]
rs55958437	0.81[EUR][1000 genomes]
rs59851071	0.81[EUR][1000 genomes]
rs61505297	1.00[EUR][1000 genomes]
rs73672189	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73672192	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73672194	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73674307	0.81[EUR][1000 genomes]
rs73674308	0.81[EUR][1000 genomes]
rs7839209	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34144800-34149200	Enhancers	Fetal Brain Male	brain
2	chr8:34146200-34148000	Enhancers	Fetal Brain Female	brain
3	chr8:34146800-34148200	Enhancers	Brain Germinal Matrix	brain

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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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