Variant report

Variant	rs12786782
Chromosome Location	chr11:34442956-34442957
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34441574..34443132-chr11:34446213..34448223,2	K562	blood:
2	chr11:34434860..34437756-chr11:34441290..34444180,2	K562	blood:
3	chr11:34436609..34439398-chr11:34442555..34445370,2	MCF-7	breast:
4	chr11:34438694..34440989-chr11:34441788..34444701,2	K562	blood:

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10768074	0.94[ASN][1000 genomes]
rs10836186	1.00[CEU][hapmap]
rs10836210	0.81[ASN][1000 genomes]
rs10836212	0.83[ASN][1000 genomes]
rs10836213	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10836214	0.94[CHB][hapmap];0.85[CHD][hapmap];0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs10836219	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10836220	0.94[JPT][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10836221	1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10836226	0.94[ASN][1000 genomes]
rs10836227	0.94[ASN][1000 genomes]
rs10836228	0.94[ASN][1000 genomes]
rs10836231	0.88[ASN][1000 genomes]
rs10836232	0.89[CHB][hapmap];0.83[CHD][hapmap];0.80[JPT][hapmap];0.87[ASN][1000 genomes]
rs10836233	0.94[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs10836235	0.87[ASN][1000 genomes]
rs11032675	0.88[EUR][1000 genomes]
rs11032677	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11032685	0.94[ASN][1000 genomes]
rs11032686	0.94[ASN][1000 genomes]
rs11032687	0.94[ASN][1000 genomes]
rs11032688	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11032689	0.89[ASN][1000 genomes]
rs11032690	0.94[ASN][1000 genomes]
rs11032691	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11032692	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11032693	0.93[ASN][1000 genomes]
rs11032694	0.93[ASN][1000 genomes]
rs11032697	0.87[ASN][1000 genomes]
rs11032701	0.87[ASN][1000 genomes]
rs11032716	0.84[ASN][1000 genomes]
rs11032717	0.81[ASN][1000 genomes]
rs12276378	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12277763	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12285367	0.94[ASN][1000 genomes]
rs12289239	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12292102	0.94[ASN][1000 genomes]
rs12708346	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12802066	0.94[ASN][1000 genomes]
rs12803540	0.84[ASN][1000 genomes]
rs1408034	0.94[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs1408036	0.94[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1408037	0.88[ASN][1000 genomes]
rs1408038	0.94[ASN][1000 genomes]
rs1408039	0.94[ASN][1000 genomes]
rs1408040	0.94[ASN][1000 genomes]
rs17881488	0.84[ASN][1000 genomes]
rs17884666	0.86[ASN][1000 genomes]
rs17885743	0.87[ASN][1000 genomes]
rs2073059	0.94[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs2223676	0.94[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2274044	0.94[CHB][hapmap];0.90[JPT][hapmap]
rs2284364	0.85[ASN][1000 genomes]
rs34682777	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3758730	0.94[CHB][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs4755368	1.00[ASW][hapmap]
rs5028597	0.97[EUR][1000 genomes]
rs60077297	0.94[ASN][1000 genomes]
rs61447308	0.94[ASN][1000 genomes]
rs6484720	0.94[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs6484721	0.88[ASN][1000 genomes]
rs7111687	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs7111765	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs7111903	1.00[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs7115206	0.90[ASN][1000 genomes]
rs7117540	0.88[ASN][1000 genomes]
rs7127109	0.94[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7127314	0.94[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7127560	0.94[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7128380	1.00[CEU][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7131159	0.88[ASN][1000 genomes]
rs7131473	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7928156	0.94[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7928368	0.94[CHB][hapmap];0.85[CHD][hapmap];0.80[JPT][hapmap];0.83[ASN][1000 genomes]
rs7928635	0.83[ASN][1000 genomes]
rs7929333	0.94[ASN][1000 genomes]
rs7929460	0.89[ASN][1000 genomes]
rs7929574	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7929828	1.00[CEU][hapmap]
rs7929899	0.94[ASN][1000 genomes]
rs7929931	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7929952	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7930070	0.94[ASN][1000 genomes]
rs7944397	0.94[CHB][hapmap];0.88[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7947841	0.94[CHB][hapmap];0.82[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.85[ASN][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	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	nsv983151	chr11:34401342-34444667	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	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:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34437200-34446200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr11:34438200-34448600	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr11:34438600-34443800	Weak transcription	Primary B cells from cord blood	blood
4	chr11:34439000-34443600	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr11:34440000-34444800	Weak transcription	Lung	lung
6	chr11:34440200-34443600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:34440200-34443800	Weak transcription	Liver	Liver
8	chr11:34440200-34447000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:34440200-34447400	Weak transcription	Hela-S3	cervix
10	chr11:34440400-34443400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr11:34440400-34443600	Weak transcription	Adipose Nuclei	Adipose
12	chr11:34440400-34443800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:34442000-34443600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr11:34442600-34443600	Enhancers	Primary neutrophils fromperipheralblood	blood

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