Variant report

Variant	rs11234273
Chromosome Location	chr11:84762531-84762532
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	chr11:84760678..84762987-chr11:84764753..84766897,2	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10501586	0.94[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs10898350	0.87[CEU][hapmap]
rs10898359	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10898360	1.00[CEU][hapmap];0.90[YRI][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10898364	0.83[CEU][hapmap]
rs11234289	1.00[YRI][hapmap];0.85[EUR][1000 genomes]
rs11823251	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1227842	0.85[CHB][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap];0.90[ASN][1000 genomes]
rs1227843	0.85[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs1238728	0.85[CHB][hapmap];0.82[JPT][hapmap];0.95[YRI][hapmap];0.90[ASN][1000 genomes]
rs1377302	1.00[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1377303	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1452928	0.82[CEU][hapmap];0.84[ASN][1000 genomes]
rs1823777	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1826613	1.00[CEU][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2453151	0.84[YRI][hapmap]
rs490286	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs4944507	0.94[CEU][hapmap]
rs542892	0.83[YRI][hapmap]
rs555259	0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];1.00[ASN][1000 genomes]
rs560214	0.82[JPT][hapmap];0.89[YRI][hapmap];0.90[ASN][1000 genomes]
rs568641	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs578782	0.82[CHB][hapmap]
rs582884	0.89[YRI][hapmap]
rs589093	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs593800	0.95[YRI][hapmap]
rs595435	0.82[JPT][hapmap];0.89[YRI][hapmap];0.90[ASN][1000 genomes]
rs601375	0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs607864	0.84[YRI][hapmap]
rs617231	0.85[CHB][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs626531	0.85[CHB][hapmap];0.84[ASN][1000 genomes]
rs630948	1.00[JPT][hapmap]
rs631370	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs633562	0.90[ASN][1000 genomes]
rs641655	0.85[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap]
rs648506	0.88[YRI][hapmap]
rs652830	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs660274	0.90[YRI][hapmap]
rs666735	0.86[YRI][hapmap]
rs675160	0.81[ASN][1000 genomes]
rs675217	0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs679745	0.85[CHB][hapmap];0.88[YRI][hapmap];0.87[ASN][1000 genomes]
rs686009	1.00[JPT][hapmap];0.95[YRI][hapmap]
rs7102107	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7110248	1.00[CEU][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7118119	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7126522	1.00[CEU][hapmap];0.84[YRI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7948646	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9634002	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9634003	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9634004	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9634018	1.00[CEU][hapmap];0.85[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948410	chr11:83918339-84812001	Bivalent/Poised TSS Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1048051	chr11:84419442-84784233	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv541109	chr11:84419442-84784233	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv430415	chr11:84661652-84833852	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1055097	chr11:84672444-84810441	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1040393	chr11:84708402-84866594	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv527535	chr11:84724795-84895033	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv528491	chr11:84724795-84895033	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv1044370	chr11:84748993-85293233	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84756400-84762800	Weak transcription	Fetal Brain Female	brain
2	chr11:84762200-84763600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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