Variant report

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11905486	1.00[ASN][1000 genomes]
rs11906214	0.95[ASN][1000 genomes]
rs11907452	1.00[ASN][1000 genomes]
rs11908191	0.81[ASN][1000 genomes]
rs12480182	1.00[ASN][1000 genomes]
rs12480424	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12480631	0.95[ASN][1000 genomes]
rs12481555	1.00[ASN][1000 genomes]
rs4239706	0.82[AFR][1000 genomes]
rs57261719	1.00[ASN][1000 genomes]
rs59917750	0.95[ASN][1000 genomes]
rs6074269	0.81[ASN][1000 genomes]
rs6074270	0.81[ASN][1000 genomes]
rs73243912	1.00[ASN][1000 genomes]
rs73243938	1.00[ASN][1000 genomes]
rs73261510	0.95[ASN][1000 genomes]
rs73261514	0.95[ASN][1000 genomes]
rs73261517	1.00[ASN][1000 genomes]
rs73261522	1.00[ASN][1000 genomes]
rs73261550	1.00[ASN][1000 genomes]
rs7345151	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8118110	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv585415	chr20:11134907-11383327	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv458869	chr20:11271614-11306751	Enhancers Weak transcription ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv585417	chr20:11271614-11306751	Weak transcription Enhancers ZNF genes & repeats	TF binding region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:11299800-11310200	Weak transcription	Pancreas	Pancrea
2	chr20:11304000-11307800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr20:11306200-11309800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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