Variant report

Variant	rs16882321
Chromosome Location	chr8:34338959-34338960
allele	A/G
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:7)

rs_ID	r²[population]
rs16881918	1.00[AMR][1000 genomes]
rs16882134	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16882210	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]
rs16882618	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	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34338600-34340200	Enhancers	Fetal Kidney	kidney

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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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