Variant report

Variant	rs11185545
Chromosome Location	chr3:196270082-196270083
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	chr3:196228123..196230544-chr3:196269103..196271110,2	MCF-7	breast:
2	chr3:196268693..196271310-chr3:196465862..196468428,2	K562	blood:

Variant related genes	Relation type
ENSG00000180370	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1124996	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11706197	0.86[AMR][1000 genomes]
rs11711594	0.82[AMR][1000 genomes]
rs12494859	0.91[AMR][1000 genomes]
rs12495687	0.91[AMR][1000 genomes]
rs2054748	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2054749	0.91[AMR][1000 genomes]
rs2054750	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2137193	0.92[AMR][1000 genomes]
rs2341334	0.80[AMR][1000 genomes]
rs28479172	0.97[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2880030	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34292861	0.85[EUR][1000 genomes]
rs4916433	0.84[EUR][1000 genomes]
rs57365032	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs60668021	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62410583	0.90[AMR][1000 genomes]
rs6583318	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs66588136	0.83[AMR][1000 genomes]
rs6799694	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6799697	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73219660	0.80[AMR][1000 genomes]
rs7615547	0.83[AMR][1000 genomes]
rs7619117	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7621684	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7626039	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9311	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9647412	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9647413	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9811428	0.94[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9813420	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9814342	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9817377	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9818507	0.83[AMR][1000 genomes]
rs9828786	0.95[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9831225	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9840938	0.80[AMR][1000 genomes]
rs9843607	0.84[EUR][1000 genomes]
rs9853777	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9854347	0.90[AMR][1000 genomes]
rs9858251	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9868492	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9870613	0.91[AMR][1000 genomes]
rs9880563	0.81[EUR][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	nsv1003194	chr3:195960270-196342423	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv536894	chr3:195960270-196342423	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	nsv1003066	chr3:196098763-196414159	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers Bivalent Enhancer Genic enhancers 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	55 gene(s)	inside rSNPs	diseases
4	esv2752687	chr3:196147690-196286690	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv948681	chr3:196148055-197007546	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
6	nsv1010483	chr3:196210054-196319543	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv536896	chr3:196210054-196319543	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv1014692	chr3:196242249-196531824	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
9	esv2763750	chr3:196242261-196278366	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv878187	chr3:196245603-196554790	Enhancers ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv491864	chr3:196263064-196468533	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
12	nsv829828	chr3:196268121-196463641	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
13	esv2511105	chr3:196269097-196270538	Inactive region	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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