Variant report

Variant	rs11720081
Chromosome Location	chr3:178693994-178693995
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:178687643..178690211-chr3:178693713..178695535,2	K562	blood:
2	chr3:178689064..178690689-chr3:178693477..178696081,2	MCF-7	breast:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs11711320	0.94[EUR][1000 genomes]
rs13072825	0.90[ASN][1000 genomes]
rs13094954	0.90[ASN][1000 genomes]
rs4245914	0.94[EUR][1000 genomes]
rs4279147	0.94[EUR][1000 genomes]
rs4280676	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4315724	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4337680	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4377525	0.93[EUR][1000 genomes]
rs4395442	0.94[EUR][1000 genomes]
rs4417911	0.94[EUR][1000 genomes]
rs4469018	0.91[EUR][1000 genomes]
rs4501160	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4505756	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4522816	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4525914	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4552405	0.94[EUR][1000 genomes]
rs4579062	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs4607155	0.87[EUR][1000 genomes]
rs4626139	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4632588	0.81[EUR][1000 genomes]
rs4637331	0.95[CEU][hapmap];0.82[EUR][1000 genomes]
rs4955796	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4955802	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4955807	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs4955810	0.94[CEU][hapmap];0.87[EUR][1000 genomes]
rs56115013	0.94[EUR][1000 genomes]
rs56154408	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6443607	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6443611	0.85[ASN][1000 genomes]
rs6443614	0.94[EUR][1000 genomes]
rs6443617	0.80[EUR][1000 genomes]
rs6772028	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs6789706	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6790867	0.94[CEU][hapmap];0.91[EUR][1000 genomes]
rs6793769	0.94[EUR][1000 genomes]
rs6793893	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs6794956	0.87[EUR][1000 genomes]
rs6795238	0.87[EUR][1000 genomes]
rs6800015	0.89[CEU][hapmap]
rs6804084	0.95[CEU][hapmap]
rs7429173	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7612363	0.94[EUR][1000 genomes]
rs7633318	0.94[CEU][hapmap]
rs7639391	0.94[CEU][hapmap];0.91[EUR][1000 genomes]
rs7643052	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7651510	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7652668	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7652946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9846511	0.94[EUR][1000 genomes]
rs9860318	0.91[EUR][1000 genomes]
rs9860749	0.91[EUR][1000 genomes]
rs9879637	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9880749	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998253	chr3:178622707-179196274	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	nsv536814	chr3:178622707-179196274	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv461026	chr3:178661814-178886609	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	nsv592649	chr3:178661814-178886609	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 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	chr3:178685200-178705200	Weak transcription	HSMMtube	muscle
2	chr3:178691400-178699600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:178692400-178699000	Weak transcription	HSMM	muscle
4	chr3:178692600-178704800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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