Variant report

Variant	rs73327130
Chromosome Location	chr8:119748062-119748063
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs61073261	1.00[AMR][1000 genomes]
rs61372731	1.00[AMR][1000 genomes]
rs73311844	1.00[AMR][1000 genomes]
rs73311846	1.00[AMR][1000 genomes]
rs73311898	1.00[AMR][1000 genomes]
rs73313868	1.00[AMR][1000 genomes]
rs73313879	1.00[AMR][1000 genomes]
rs73313898	1.00[AMR][1000 genomes]
rs73315516	1.00[AMR][1000 genomes]
rs73317569	1.00[AMR][1000 genomes]
rs73319370	1.00[AMR][1000 genomes]
rs73319393	1.00[AMR][1000 genomes]
rs73325086	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7815228	1.00[AMR][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	nsv465786	chr8:119627671-119767165	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv612048	chr8:119627671-119767165	Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr8:119744400-119755600	Weak transcription	Aorta	Aorta

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

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