Variant report

Variant	rs16882210
Chromosome Location	chr8:34311816-34311817
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs16881918	1.00[AMR][1000 genomes]
rs16882134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16882321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16882355	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16882589	1.00[AMR][1000 genomes]
rs1838581	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3421299	chr8:34311710-34315908	Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34311800-34312000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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