Variant report

Variant	rs4923305
Chromosome Location	chr11:25802227-25802228
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1038932	0.81[ASN][1000 genomes]
rs1038933	0.81[ASN][1000 genomes]
rs1038934	0.81[ASN][1000 genomes]
rs1038937	0.84[ASN][1000 genomes]
rs1038938	0.84[ASN][1000 genomes]
rs10501024	0.87[ASN][1000 genomes]
rs10767439	0.84[ASN][1000 genomes]
rs10767448	0.87[ASN][1000 genomes]
rs10767449	0.87[ASN][1000 genomes]
rs10767450	0.87[ASN][1000 genomes]
rs10834774	0.84[ASN][1000 genomes]
rs11028881	0.81[ASN][1000 genomes]
rs11028888	0.84[ASN][1000 genomes]
rs11028889	0.84[ASN][1000 genomes]
rs11028890	0.84[ASN][1000 genomes]
rs11028893	0.84[ASN][1000 genomes]
rs11028903	0.84[ASN][1000 genomes]
rs11028904	0.84[ASN][1000 genomes]
rs11028905	0.84[ASN][1000 genomes]
rs11028919	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11028925	0.98[ASN][1000 genomes]
rs11028926	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11028927	0.98[ASN][1000 genomes]
rs1121664	0.94[ASN][1000 genomes]
rs1158052	0.87[ASN][1000 genomes]
rs11601475	0.85[ASN][1000 genomes]
rs12271018	0.81[ASN][1000 genomes]
rs12271021	0.81[ASN][1000 genomes]
rs12291285	0.80[ASN][1000 genomes]
rs12360774	0.81[ASN][1000 genomes]
rs12363608	0.81[ASN][1000 genomes]
rs1389421	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1389422	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1493663	0.87[ASN][1000 genomes]
rs1493676	0.94[ASN][1000 genomes]
rs1493679	0.84[ASN][1000 genomes]
rs1532287	0.94[ASN][1000 genomes]
rs1532288	0.94[ASN][1000 genomes]
rs1845335	0.85[ASN][1000 genomes]
rs1908163	0.81[ASN][1000 genomes]
rs1908164	0.84[ASN][1000 genomes]
rs1908165	0.84[ASN][1000 genomes]
rs1908166	0.84[ASN][1000 genomes]
rs1908167	0.84[ASN][1000 genomes]
rs2131663	0.84[ASN][1000 genomes]
rs2172581	0.84[ASN][1000 genomes]
rs4923300	0.87[ASN][1000 genomes]
rs4923303	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4923304	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56375749	0.81[ASN][1000 genomes]
rs6484170	0.84[ASN][1000 genomes]
rs6484171	0.87[ASN][1000 genomes]
rs6484172	0.87[ASN][1000 genomes]
rs7108839	0.84[ASN][1000 genomes]
rs7127101	0.83[ASN][1000 genomes]
rs7935615	0.81[ASN][1000 genomes]
rs7935620	0.81[ASN][1000 genomes]
rs7938971	0.81[ASN][1000 genomes]
rs7939196	0.81[ASN][1000 genomes]
rs7939236	0.81[ASN][1000 genomes]
rs7944052	0.94[ASN][1000 genomes]
rs961923	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9804685	0.81[ASN][1000 genomes]
rs9804687	0.81[ASN][1000 genomes]
rs984830	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760599	chr11:25186984-26159450	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1046507	chr11:25469712-26111707	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2759811	chr11:25564190-25842666	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1041080	chr11:25585107-25931087	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1039190	chr11:25592509-25925352	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv540973	chr11:25592509-25925352	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	esv2758259	chr11:25633803-25842666	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv428252	chr11:25633803-25842666	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv467774	chr11:25773322-25924809	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv553895	chr11:25773322-25924809	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv1050179	chr11:25793308-25816730	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv897138	chr11:25801048-25861113	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	nsv897139	chr11:25801048-25861113	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:25802000-25803800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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