Variant report

Variant	rs7814068
Chromosome Location	chr8:9704853-9704854
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11249963	0.83[ASN][1000 genomes]
rs12114977	0.83[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs12540961	0.89[EUR][1000 genomes]
rs12547274	0.89[EUR][1000 genomes]
rs12550323	0.89[EUR][1000 genomes]
rs13251619	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13260533	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7823438	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9644712	0.83[ASN][1000 genomes]
rs9657510	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530864	chr8:9097498-9914548	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv16865	chr8:9642195-9712807	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 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	chr8:9704800-9707200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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