Variant report

Variant	rs11182771
Chromosome Location	chr12:45366870-45366871
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:45356113..45357820-chr12:45366859..45369459,2	K562	blood:
2	chr12:45366332..45368097-chr12:45514780..45516888,12	MCF-7	breast:
3	chr12:45366306..45367231-chr12:45516422..45517207,2	MCF-7	breast:

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs10506259	1.00[AMR][1000 genomes]
rs10880694	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs10880698	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs10880699	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs10880727	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10880728	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10880729	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10880731	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182700	0.89[AMR][1000 genomes]
rs11182704	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs11182709	1.00[AMR][1000 genomes]
rs11182712	1.00[AMR][1000 genomes]
rs11182713	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs11182714	1.00[CEU][hapmap];0.93[CHB][hapmap];0.91[JPT][hapmap];1.00[AMR][1000 genomes]
rs11182717	1.00[AMR][1000 genomes]
rs11182722	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs11182724	1.00[AMR][1000 genomes]
rs11182725	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs11182729	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs11182730	1.00[AMR][1000 genomes]
rs11182732	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs11182770	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182772	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11182785	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11182789	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11182790	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11182791	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11182792	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11182793	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11182796	1.00[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182798	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182806	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182807	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182808	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182809	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11182812	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11534985	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs12227311	1.00[AMR][1000 genomes]
rs12227622	0.93[CHB][hapmap];0.89[AMR][1000 genomes]
rs12228073	0.93[CHB][hapmap];1.00[AMR][1000 genomes]
rs12228476	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs12578220	1.00[CEU][hapmap]
rs12579006	1.00[EUR][1000 genomes]
rs12580287	1.00[AMR][1000 genomes]
rs12580562	1.00[EUR][1000 genomes]
rs12581554	1.00[CEU][hapmap]
rs12581653	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12581852	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12581880	1.00[EUR][1000 genomes]
rs12581903	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes]
rs12582602	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12829945	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17095196	1.00[AMR][1000 genomes]
rs17095198	1.00[AMR][1000 genomes]
rs17095247	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs17095441	1.00[CEU][hapmap]
rs2658976	0.87[CHB][hapmap]
rs2703049	1.00[CEU][hapmap]
rs2703052	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs2710418	1.00[CEU][hapmap];0.93[CHB][hapmap];0.85[JPT][hapmap]
rs2710424	0.87[CHB][hapmap]
rs3803172	1.00[EUR][1000 genomes]
rs3803174	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3803175	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs447760	0.88[CHB][hapmap]
rs57726055	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59646766	1.00[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs7295338	0.82[CHB][hapmap]
rs7300104	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7315817	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7968450	1.00[CEU][hapmap]

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	nsv899049	chr12:45299202-45376053	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv899050	chr12:45299202-45400614	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv899051	chr12:45307633-45376053	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
4	esv3407092	chr12:45342734-45368068	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv3351644	chr12:45345597-45529449	Bivalent Enhancer Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1045857	chr12:45351172-45468784	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv541485	chr12:45351172-45468784	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv469365	chr12:45353367-45388817	Enhancers Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv558751	chr12:45353367-45388817	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv469366	chr12:45357804-45386398	Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv558752	chr12:45357804-45386398	Enhancers Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv469367	chr12:45363545-45400614	Enhancers Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv558753	chr12:45363545-45400614	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	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	chr12:45366800-45367200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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