Variant report

Variant	rs6989408
Chromosome Location	chr8:64696385-64696386
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1216549	1.00[EUR][1000 genomes]
rs16930569	1.00[ASN][1000 genomes]
rs16930572	1.00[ASN][1000 genomes]
rs56288719	1.00[ASN][1000 genomes]
rs58364107	1.00[ASN][1000 genomes]
rs60751598	1.00[ASN][1000 genomes]
rs72649264	1.00[ASN][1000 genomes]
rs72649267	1.00[ASN][1000 genomes]
rs72649293	1.00[ASN][1000 genomes]
rs72651204	1.00[ASN][1000 genomes]
rs72651220	1.00[ASN][1000 genomes]
rs73269092	1.00[ASN][1000 genomes]
rs7818563	1.00[ASN][1000 genomes]
rs7818697	1.00[ASN][1000 genomes]
rs791394	1.00[EUR][1000 genomes]
rs791397	1.00[EUR][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	nsv831344	chr8:64658229-64712338	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr8:64691200-64700800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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