Variant report

Variant	rs56308637
Chromosome Location	chr3:135639648-135639649
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:135637277..135640102-chr3:135755652..135757448,2	MCF-7	breast:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10048942	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10049233	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs10512981	0.85[ASN][1000 genomes]
rs10935175	0.92[ASN][1000 genomes]
rs13082684	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13322891	1.00[ASN][1000 genomes]
rs13434196	0.85[ASN][1000 genomes]
rs1356664	1.00[ASN][1000 genomes]
rs1401545	1.00[ASN][1000 genomes]
rs1403766	1.00[ASN][1000 genomes]
rs1403767	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1403770	0.92[ASN][1000 genomes]
rs1568349	0.85[ASN][1000 genomes]
rs1568350	1.00[ASN][1000 genomes]
rs16843509	0.85[ASN][1000 genomes]
rs2204259	0.85[ASN][1000 genomes]
rs28449384	0.92[ASN][1000 genomes]
rs28570106	1.00[ASN][1000 genomes]
rs28576629	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28855968	1.00[ASN][1000 genomes]
rs28875187	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34522617	0.92[ASN][1000 genomes]
rs34767379	0.92[ASN][1000 genomes]
rs35722356	1.00[ASN][1000 genomes]
rs36039354	0.92[ASN][1000 genomes]
rs4718	1.00[ASN][1000 genomes]
rs55678980	1.00[ASN][1000 genomes]
rs56807950	0.85[ASN][1000 genomes]
rs59063369	0.85[ASN][1000 genomes]
rs66544356	0.85[ASN][1000 genomes]
rs6773469	0.85[ASN][1000 genomes]
rs6775778	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6779603	0.85[ASN][1000 genomes]
rs6802139	0.85[ASN][1000 genomes]
rs6807058	0.92[ASN][1000 genomes]
rs6807565	0.92[ASN][1000 genomes]
rs73222222	0.92[ASN][1000 genomes]
rs7427833	0.92[ASN][1000 genomes]
rs7433567	0.92[ASN][1000 genomes]
rs7609938	0.85[ASN][1000 genomes]
rs7621396	0.92[ASN][1000 genomes]
rs7626676	0.85[ASN][1000 genomes]
rs7628848	0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7638129	0.85[ASN][1000 genomes]
rs7640153	0.85[ASN][1000 genomes]
rs7641070	0.92[ASN][1000 genomes]
rs870812	1.00[ASN][1000 genomes]
rs908825	1.00[ASN][1000 genomes]
rs9813082	0.85[ASN][1000 genomes]
rs9814505	1.00[ASN][1000 genomes]
rs9814557	0.92[ASN][1000 genomes]
rs9819440	1.00[ASN][1000 genomes]
rs9819988	0.85[ASN][1000 genomes]
rs9820189	1.00[ASN][1000 genomes]
rs9824558	0.85[ASN][1000 genomes]
rs9825239	0.92[ASN][1000 genomes]
rs9827662	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9829329	0.85[ASN][1000 genomes]
rs9829476	0.85[ASN][1000 genomes]
rs9833699	1.00[ASN][1000 genomes]
rs9833799	0.85[ASN][1000 genomes]
rs9834624	1.00[ASN][1000 genomes]
rs9836758	0.92[ASN][1000 genomes]
rs9837855	1.00[ASN][1000 genomes]
rs9839259	0.85[ASN][1000 genomes]
rs9842864	0.92[ASN][1000 genomes]
rs9843725	0.92[ASN][1000 genomes]
rs9844478	0.85[ASN][1000 genomes]
rs9848322	0.92[ASN][1000 genomes]
rs9849088	0.85[ASN][1000 genomes]
rs9852406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9854494	1.00[ASN][1000 genomes]
rs9862777	0.92[ASN][1000 genomes]
rs9864656	0.85[ASN][1000 genomes]
rs9864775	1.00[ASN][1000 genomes]
rs9870581	1.00[ASN][1000 genomes]
rs9875948	1.00[ASN][1000 genomes]
rs9876837	0.85[ASN][1000 genomes]
rs9877722	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460860	chr3:135107678-135769006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv591829	chr3:135107678-135769006	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv829732	chr3:135561706-135756840	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135636200-135640400	Weak transcription	Pancreas	Pancrea
2	chr3:135636200-135640600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr3:135636200-135641400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr3:135636400-135641600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:135636600-135640800	Weak transcription	NHEK	skin

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