Variant report

Variant	rs11032697
Chromosome Location	chr11:34456711-34456712
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34452131..34454607-chr11:34455028..34457800,3	K562	blood:
2	chr11:34452352..34457130-chr11:34458043..34461797,6	K562	blood:
3	chr11:34451992..34454656-chr11:34455996..34457746,2	MCF-7	breast:
4	chr11:34456171..34458187-chr11:34459841..34462711,2	MCF-7	breast:
5	chr11:34452850..34454607-chr11:34455028..34457800,2	K562	blood:

Variant related genes	Relation type
ENSG00000216708	Chromatin interaction
ENSG00000121691	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10768074	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10836212	0.82[ASN][1000 genomes]
rs10836213	0.82[ASN][1000 genomes]
rs10836214	0.82[ASN][1000 genomes]
rs10836219	0.87[ASN][1000 genomes]
rs10836220	0.87[ASN][1000 genomes]
rs10836221	0.87[ASN][1000 genomes]
rs10836226	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10836227	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10836228	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10836231	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836232	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836233	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836235	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11032677	0.89[ASN][1000 genomes]
rs11032685	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032686	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032687	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032688	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032689	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11032690	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032691	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032692	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11032693	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11032694	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11032701	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11032716	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11032717	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11608027	0.81[EUR][1000 genomes]
rs12276378	0.87[ASN][1000 genomes]
rs12277763	0.87[ASN][1000 genomes]
rs12285367	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12289239	0.87[ASN][1000 genomes]
rs12292102	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12708346	0.82[ASN][1000 genomes]
rs12786782	0.87[ASN][1000 genomes]
rs12802066	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12803540	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1408034	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1408036	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1408037	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1408038	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1408039	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1408040	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17881488	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17884666	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17885743	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2073059	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2223676	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2284364	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2420387	0.81[EUR][1000 genomes]
rs34682777	0.87[ASN][1000 genomes]
rs3758730	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60077297	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61447308	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6484720	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6484721	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7111687	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7111765	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7111903	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7115206	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7117384	0.91[ASN][1000 genomes]
rs7117540	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7118388	0.82[ASN][1000 genomes]
rs7127109	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7127314	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7127560	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7131159	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7131473	0.91[ASN][1000 genomes]
rs7928156	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7928368	0.82[ASN][1000 genomes]
rs7928635	0.82[ASN][1000 genomes]
rs7929333	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7929460	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7929574	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7929899	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7929931	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7929952	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7930070	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7944397	0.94[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7947841	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897205	chr11:34248229-34507213	Enhancers Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv897207	chr11:34253683-34621004	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv897208	chr11:34257064-34562247	Strong transcription Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv897209	chr11:34309519-34548906	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv832114	chr11:34424428-34607851	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34443800-34460000	Weak transcription	Esophagus	oesophagus
2	chr11:34449400-34459600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr11:34449600-34459200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:34450000-34457600	Weak transcription	NHDF-Ad	bronchial
5	chr11:34451200-34457800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:34453800-34457600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:34453800-34459000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr11:34453800-34459200	Weak transcription	Adipose Nuclei	Adipose
9	chr11:34454000-34459000	Weak transcription	Primary B cells from cord blood	blood
10	chr11:34454800-34460000	Weak transcription	Lung	lung
11	chr11:34455000-34457400	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr11:34455000-34457400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr11:34455000-34457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:34455000-34457800	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr11:34456000-34457400	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr11:34456000-34460000	Weak transcription	Pancreas	Pancrea
17	chr11:34456200-34457400	Weak transcription	K562	blood
18	chr11:34456400-34457400	Weak transcription	Liver	Liver
19	chr11:34456400-34459800	Weak transcription	HepG2	liver

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