Variant report

Variant	rs11670865
Chromosome Location	chr19:41531522-41531523
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1038376	0.95[CEU][hapmap];0.91[CHB][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10401226	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10402037	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10402070	0.92[AFR][1000 genomes]
rs10402611	0.92[AFR][1000 genomes]
rs10403140	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10403268	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10403330	0.92[AFR][1000 genomes]
rs10409701	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10409738	0.92[AFR][1000 genomes]
rs10410347	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10410867	0.92[AFR][1000 genomes]
rs10413524	0.92[AFR][1000 genomes]
rs10415473	0.92[AFR][1000 genomes]
rs10417678	0.92[AFR][1000 genomes]
rs10418426	0.87[AFR][1000 genomes]
rs10418473	0.88[AFR][1000 genomes]
rs10418657	0.89[AFR][1000 genomes]
rs10419098	0.92[AFR][1000 genomes]
rs10419321	0.94[AFR][1000 genomes]
rs10420699	0.94[AFR][1000 genomes]
rs10421597	0.92[AFR][1000 genomes]
rs10421834	0.92[AFR][1000 genomes]
rs10422151	0.92[AFR][1000 genomes]
rs10422282	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10422729	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs10422829	0.92[AFR][1000 genomes]
rs10423743	1.00[YRI][hapmap];0.92[AFR][1000 genomes]
rs10424716	0.94[AFR][1000 genomes]
rs10424952	0.81[AFR][1000 genomes]
rs10425384	0.88[AFR][1000 genomes]
rs10426482	0.82[AFR][1000 genomes]
rs10500282	0.81[CEU][hapmap]
rs1080234	0.92[AFR][1000 genomes]
rs1080235	0.92[AFR][1000 genomes]
rs11083596	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11667928	0.84[AFR][1000 genomes]
rs11667976	1.00[YRI][hapmap]
rs11671743	0.91[AFR][1000 genomes]
rs11673685	0.91[AFR][1000 genomes]
rs11879790	0.94[AFR][1000 genomes]
rs16974878	0.92[AFR][1000 genomes]
rs1807967	0.92[AFR][1000 genomes]
rs2054675	0.85[CEU][hapmap]
rs28671673	0.92[AFR][1000 genomes]
rs3745274	0.81[CEU][hapmap]
rs3745275	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7249735	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7254767	0.94[AFR][1000 genomes]
rs8103372	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758500	chr19:41291627-41546068	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2758762	chr19:41291627-41546068	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv1066637	chr19:41309211-41597896	Weak transcription Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	esv3337314	chr19:41388910-41534583	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	esv2755485	chr19:41431935-41558271	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1058051	chr19:41497274-41558271	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1065684	chr19:41516389-41644542	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv978817	chr19:41530217-41531640	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41524600-41531800	Weak transcription	Liver	Liver
2	chr19:41529400-41531800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:41530200-41534000	Weak transcription	Right Atrium	heart
4	chr19:41531200-41531800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:41531400-41532000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:41531400-41532200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast

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