Variant report

Variant	rs11821389
Chromosome Location	chr11:27120081-27120082
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs1020269	1.00[CHB][hapmap]
rs1044273	0.93[CEU][hapmap]
rs10501076	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10501079	1.00[ASN][1000 genomes]
rs10767601	1.00[CHB][hapmap]
rs10767604	1.00[CHB][hapmap]
rs10767609	0.93[CEU][hapmap]
rs10835114	1.00[CHB][hapmap]
rs10835118	1.00[CHB][hapmap]
rs11029827	0.93[CEU][hapmap]
rs11029833	0.93[CEU][hapmap]
rs11511900	0.90[CEU][hapmap]
rs11602261	0.93[CEU][hapmap]
rs11605939	0.93[CEU][hapmap]
rs12099199	1.00[ASN][1000 genomes]
rs12099200	1.00[ASN][1000 genomes]
rs1317726	1.00[CHB][hapmap];0.84[AFR][1000 genomes]
rs1372903	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1442918	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1442937	0.95[ASN][1000 genomes]
rs1442942	0.80[AFR][1000 genomes]
rs1470270	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16916613	1.00[ASN][1000 genomes]
rs16916618	1.00[ASN][1000 genomes]
rs16916620	1.00[ASN][1000 genomes]
rs16916630	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs16916633	1.00[ASN][1000 genomes]
rs16916634	1.00[ASN][1000 genomes]
rs16925452	1.00[ASN][1000 genomes]
rs17243908	1.00[ASN][1000 genomes]
rs17243943	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17243951	0.96[ASN][1000 genomes]
rs17309642	1.00[ASN][1000 genomes]
rs17309656	0.93[CEU][hapmap]
rs17309677	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17309691	1.00[ASN][1000 genomes]
rs1899507	1.00[ASN][1000 genomes]
rs1899508	1.00[ASN][1000 genomes]
rs2002082	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2002083	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2015158	1.00[ASN][1000 genomes]
rs2015372	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2099887	1.00[CHB][hapmap]
rs2197189	1.00[ASN][1000 genomes]
rs2197193	1.00[ASN][1000 genomes]
rs2304912	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2304913	1.00[ASN][1000 genomes]
rs3183973	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3802783	1.00[ASN][1000 genomes]
rs4278476	0.93[CEU][hapmap]
rs4328173	0.93[CEU][hapmap]
rs4409779	1.00[ASN][1000 genomes]
rs4426092	1.00[ASN][1000 genomes]
rs4450135	1.00[ASN][1000 genomes]
rs4603260	1.00[ASN][1000 genomes]
rs4620678	1.00[ASN][1000 genomes]
rs4923423	0.93[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs4923424	1.00[CHB][hapmap];0.82[LWK][hapmap]
rs55635960	1.00[ASN][1000 genomes]
rs56932826	1.00[ASN][1000 genomes]
rs57495929	0.96[ASN][1000 genomes]
rs58106325	1.00[ASN][1000 genomes]
rs58124167	1.00[ASN][1000 genomes]
rs58156212	1.00[ASN][1000 genomes]
rs58308268	1.00[ASN][1000 genomes]
rs59045289	1.00[ASN][1000 genomes]
rs59643797	1.00[ASN][1000 genomes]
rs59753371	0.91[ASN][1000 genomes]
rs59945650	1.00[ASN][1000 genomes]
rs60376193	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60428745	1.00[ASN][1000 genomes]
rs60551343	1.00[ASN][1000 genomes]
rs61106295	1.00[ASN][1000 genomes]
rs61116911	1.00[ASN][1000 genomes]
rs7113071	1.00[CHB][hapmap]
rs7124528	1.00[CHB][hapmap];0.85[AFR][1000 genomes]
rs7129825	0.91[AFR][1000 genomes]
rs727838	0.96[ASN][1000 genomes]
rs73434077	1.00[ASN][1000 genomes]
rs73434081	1.00[ASN][1000 genomes]
rs73434083	1.00[ASN][1000 genomes]
rs73435913	1.00[ASN][1000 genomes]
rs7925797	0.93[CEU][hapmap]
rs7930844	1.00[CHB][hapmap];0.80[AFR][1000 genomes]
rs7931643	1.00[CHB][hapmap]
rs7943507	1.00[ASN][1000 genomes]
rs7949619	0.84[ASW][hapmap];0.93[CEU][hapmap];0.84[LWK][hapmap];0.81[MKK][hapmap];1.00[YRI][hapmap]
rs972904	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.94[LWK][hapmap];0.93[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs985597	0.93[CEU][hapmap]
rs987687	0.93[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916187	chr11:26576875-27328603	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv949332	chr11:26935972-27223492	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv897147	chr11:26983363-27258899	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1040964	chr11:26998213-27223388	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv540975	chr11:26998213-27223388	Enhancers Bivalent Enhancer Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv949575	chr11:27005687-27233359	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv533052	chr11:27006061-27225374	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv553912	chr11:27014032-27240951	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv467781	chr11:27019331-27240951	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv553913	chr11:27019331-27240951	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:27110800-27137000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:27118800-27122400	Weak transcription	Esophagus	oesophagus

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