Variant report

Variant	rs7648725
Chromosome Location	chr3:158943384-158943385
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs2365480	1.00[EUR][1000 genomes]
rs2365481	1.00[EUR][1000 genomes]
rs55989643	1.00[EUR][1000 genomes]
rs56680876	1.00[EUR][1000 genomes]
rs56791207	1.00[EUR][1000 genomes]
rs57279778	1.00[EUR][1000 genomes]
rs57789957	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59076814	1.00[AMR][1000 genomes]
rs59185941	1.00[EUR][1000 genomes]
rs59229685	1.00[EUR][1000 genomes]
rs6793688	1.00[EUR][1000 genomes]
rs73877533	1.00[EUR][1000 genomes]
rs73877535	1.00[EUR][1000 genomes]
rs73877536	1.00[EUR][1000 genomes]
rs73877541	1.00[EUR][1000 genomes]
rs73877542	1.00[EUR][1000 genomes]
rs73877543	1.00[EUR][1000 genomes]
rs73877546	1.00[EUR][1000 genomes]
rs73877548	1.00[EUR][1000 genomes]
rs7628986	1.00[EUR][1000 genomes]
rs7629391	0.91[LWK][hapmap];1.00[MKK][hapmap]
rs7650928	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7651706	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530059	chr3:158332590-159147549	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv470971	chr3:158590928-159158217	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv3426016	chr3:158676623-158979242	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv491927	chr3:158692653-158952780	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1012602	chr3:158800182-159031618	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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