Variant report

Variant	rs58140595
Chromosome Location	chr3:139955894-139955895
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11918688	1.00[EUR][1000 genomes]
rs11924457	1.00[EUR][1000 genomes]
rs11927090	1.00[EUR][1000 genomes]
rs1383020	1.00[EUR][1000 genomes]
rs16850133	1.00[EUR][1000 genomes]
rs2061927	1.00[EUR][1000 genomes]
rs2061928	1.00[EUR][1000 genomes]
rs2086330	1.00[EUR][1000 genomes]
rs34648747	1.00[EUR][1000 genomes]
rs4142786	1.00[EUR][1000 genomes]
rs4234485	1.00[EUR][1000 genomes]
rs4263252	1.00[EUR][1000 genomes]
rs4365587	1.00[EUR][1000 genomes]
rs4438621	1.00[EUR][1000 genomes]
rs4518083	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56834107	1.00[EUR][1000 genomes]
rs57193140	1.00[EUR][1000 genomes]
rs57563861	1.00[EUR][1000 genomes]
rs57865055	1.00[EUR][1000 genomes]
rs59385932	1.00[EUR][1000 genomes]
rs61015005	1.00[EUR][1000 genomes]
rs6439914	1.00[EUR][1000 genomes]
rs6765087	1.00[EUR][1000 genomes]
rs6773144	1.00[EUR][1000 genomes]
rs72990191	1.00[EUR][1000 genomes]
rs72990200	1.00[EUR][1000 genomes]
rs73867103	1.00[EUR][1000 genomes]
rs73867105	1.00[EUR][1000 genomes]
rs73867110	1.00[EUR][1000 genomes]
rs73870712	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73870714	1.00[EUR][1000 genomes]
rs73870715	1.00[EUR][1000 genomes]
rs7610342	0.86[EUR][1000 genomes]
rs7626588	1.00[EUR][1000 genomes]
rs7638929	1.00[EUR][1000 genomes]
rs995578	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	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv432486	chr3:139924092-140049121	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv2757891	chr3:139925764-140524730	Enhancers Weak transcription Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv2759181	chr3:139925764-140524730	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv829740	chr3:139925767-140106169	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv527831	chr3:139932966-140533823	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139954600-139959400	Weak transcription	Pancreas	Pancrea
2	chr3:139954600-139961600	Weak transcription	Ovary	ovary
3	chr3:139954800-139961400	Weak transcription	HSMMtube	muscle
4	chr3:139955600-139956400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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