Variant report

Variant	rs8010334
Chromosome Location	chr14:32659697-32659698
allele	A/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]
rs10483395	0.81[EUR][1000 genomes]
rs10483396	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7151266	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72664675	0.81[EUR][1000 genomes]
rs72664682	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8013272	0.82[EUR][1000 genomes];0.83[ASN][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	nsv832764	chr14:32564468-32723213	Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32659200-32660400	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr14:32659400-32660200	Enhancers	Primary B cells from peripheral blood	blood

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

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