Variant report

Variant	rs16882098
Chromosome Location	chr8:34250055-34250056
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10503958	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10503963	0.95[AMR][1000 genomes]
rs1562183	0.85[ASN][1000 genomes]
rs16882013	0.83[ASN][1000 genomes]
rs16882016	0.83[ASN][1000 genomes]
rs16882072	0.86[ASN][1000 genomes]
rs4289807	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4739475	1.00[EUR][1000 genomes]
rs4739543	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4739588	0.85[AMR][1000 genomes]
rs60730442	0.85[ASN][1000 genomes]
rs716225	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs73674310	0.81[ASN][1000 genomes]
rs73674323	0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34250000-34251000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr8:34250000-34251800	Enhancers	Colon Smooth Muscle	Colon

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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