Variant report

Variant	rs13093154
Chromosome Location	chr3:155836231-155836232
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10936024	0.94[CHB][hapmap];0.84[JPT][hapmap];0.91[ASN][1000 genomes]
rs11709514	0.94[CHB][hapmap];0.85[JPT][hapmap];0.88[ASN][1000 genomes]
rs11716256	0.95[ASN][1000 genomes]
rs11718399	0.94[CHB][hapmap];0.97[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs13073556	0.94[CHB][hapmap];0.97[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1488425	0.94[CHB][hapmap];0.97[CHD][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs1488426	0.91[ASN][1000 genomes]
rs1984473	0.83[CHB][hapmap]
rs4234308	0.80[CHB][hapmap];0.83[ASN][1000 genomes]
rs4261831	0.94[CHB][hapmap];0.91[JPT][hapmap];0.93[ASN][1000 genomes]
rs4359773	0.84[ASN][1000 genomes]
rs4359774	0.83[CHB][hapmap];0.84[ASN][1000 genomes]
rs4605502	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs4679760	0.84[ASN][1000 genomes]
rs4679761	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs4680232	0.94[CHB][hapmap];0.97[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs4680233	0.94[CHB][hapmap];0.84[JPT][hapmap];0.91[ASN][1000 genomes]
rs4680234	0.89[ASN][1000 genomes]
rs4680235	0.89[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs4680237	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs56231269	0.89[ASN][1000 genomes]
rs62284939	0.90[ASN][1000 genomes]
rs6441034	0.89[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs6441035	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs6441036	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs6761966	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs6778035	0.94[CHB][hapmap];0.92[JPT][hapmap]
rs6780500	0.91[ASN][1000 genomes]
rs6788449	0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6793964	0.94[CHB][hapmap];0.89[ASN][1000 genomes]
rs7613000	0.81[ASN][1000 genomes]
rs7617796	0.94[CHB][hapmap];0.92[JPT][hapmap];0.93[ASN][1000 genomes]
rs7618820	0.81[CHB][hapmap];0.84[ASN][1000 genomes]
rs7629439	0.89[CHB][hapmap];0.81[ASN][1000 genomes]
rs7633081	0.93[ASN][1000 genomes]
rs9289961	0.94[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs9814661	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs9816126	0.89[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs9838322	0.94[CHB][hapmap];0.92[JPT][hapmap];0.87[ASN][1000 genomes]
rs9842620	0.94[CHB][hapmap];0.97[CHD][hapmap];0.92[JPT][hapmap];0.92[ASN][1000 genomes]
rs9856468	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs9861320	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs9862153	0.94[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs9869649	0.94[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs9870793	0.83[ASN][1000 genomes]
rs9882088	0.88[CHB][hapmap];0.81[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	nsv592085	chr3:155827634-156012679	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr3:155835200-155836600	Weak transcription	Pancreas	Pancrea

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