Variant report

Variant	rs11011364
Chromosome Location	chr10:38065887-38065888
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	chr10:38063395..38067055-chr10:38144892..38148100,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000198105	Chromatin interaction
ENSG00000236514	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10827830	1.00[EUR][1000 genomes]
rs10827834	1.00[EUR][1000 genomes]
rs10827837	1.00[EUR][1000 genomes]
rs10827838	1.00[EUR][1000 genomes]
rs11011356	1.00[EUR][1000 genomes]
rs11011368	0.89[EUR][1000 genomes]
rs11011375	1.00[EUR][1000 genomes]
rs11011376	0.82[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11011385	1.00[EUR][1000 genomes]
rs11011393	1.00[EUR][1000 genomes]
rs11011403	1.00[EUR][1000 genomes]
rs11011412	1.00[EUR][1000 genomes]
rs11011415	1.00[EUR][1000 genomes]
rs11812927	1.00[EUR][1000 genomes]
rs11814622	1.00[EUR][1000 genomes]
rs11816307	1.00[EUR][1000 genomes]
rs11817696	1.00[EUR][1000 genomes]
rs11818933	1.00[EUR][1000 genomes]
rs11819551	1.00[EUR][1000 genomes]
rs12240311	0.85[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12244864	1.00[EUR][1000 genomes]
rs12248857	1.00[EUR][1000 genomes]
rs12250395	1.00[EUR][1000 genomes]
rs12251570	1.00[EUR][1000 genomes]
rs12252091	0.89[EUR][1000 genomes]
rs12252754	1.00[EUR][1000 genomes]
rs12256181	1.00[EUR][1000 genomes]
rs12256794	1.00[EUR][1000 genomes]
rs12257632	1.00[EUR][1000 genomes]
rs12258024	1.00[EUR][1000 genomes]
rs12258128	1.00[EUR][1000 genomes]
rs12258252	0.82[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12260310	1.00[EUR][1000 genomes]
rs12262559	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12262814	1.00[EUR][1000 genomes]
rs12262927	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12267847	1.00[EUR][1000 genomes]
rs12267923	1.00[EUR][1000 genomes]
rs12770231	1.00[EUR][1000 genomes]
rs12770438	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12778900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12779056	1.00[EUR][1000 genomes]
rs12783599	1.00[EUR][1000 genomes]
rs34152840	1.00[EUR][1000 genomes]
rs34222428	1.00[EUR][1000 genomes]
rs34591573	1.00[EUR][1000 genomes]
rs34724357	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34964888	1.00[EUR][1000 genomes]
rs35006520	1.00[EUR][1000 genomes]
rs35056062	1.00[EUR][1000 genomes]
rs35246660	1.00[EUR][1000 genomes]
rs35404142	1.00[EUR][1000 genomes]
rs35818588	1.00[EUR][1000 genomes]
rs57753536	1.00[EUR][1000 genomes]
rs60538050	1.00[EUR][1000 genomes]
rs71491203	1.00[EUR][1000 genomes]
rs71491210	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71491212	1.00[EUR][1000 genomes]
rs71491214	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895030	chr10:37715737-38674609	Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1045684	chr10:37765361-38426204	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv540564	chr10:37765361-38426204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1040704	chr10:37940024-38451917	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
5	nsv975812	chr10:37990724-38084639	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv947608	chr10:38053801-38066317	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:38047000-38069400	Weak transcription	Ovary	ovary
2	chr10:38051800-38066000	Weak transcription	HepG2	liver
3	chr10:38065400-38066400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
4	chr10:38065400-38066400	Enhancers	Dnd41	blood

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