Variant report

Variant	rs7110248
Chromosome Location	chr11:84789357-84789358
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	chr11:84787875..84791541-chr11:84796129..84798361,4	MCF-7	breast:
2	chr11:84789051..84790870-chr11:84792709..84795288,2	MCF-7	breast:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10501586	0.94[CEU][hapmap]
rs10792794	0.93[YRI][hapmap]
rs10898350	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs10898359	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10898360	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898364	0.83[CEU][hapmap]
rs11234273	1.00[CEU][hapmap];0.82[YRI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11234289	0.80[YRI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11823251	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1227842	0.82[CHB][hapmap]
rs1227843	0.82[CHB][hapmap]
rs1238728	0.82[CHB][hapmap]
rs1377302	1.00[CEU][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1377303	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1452928	0.82[CEU][hapmap]
rs1823777	1.00[CEU][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1826613	1.00[CEU][hapmap];0.80[YRI][hapmap];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2453151	1.00[JPT][hapmap];0.88[YRI][hapmap];0.88[ASN][1000 genomes]
rs2513242	0.94[ASN][1000 genomes]
rs4944507	0.94[CEU][hapmap];1.00[JPT][hapmap]
rs540153	0.81[ASN][1000 genomes]
rs542892	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs543740	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs555156	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs555259	1.00[YRI][hapmap]
rs560214	0.93[YRI][hapmap]
rs567594	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs568330	0.97[ASN][1000 genomes]
rs582884	0.80[YRI][hapmap]
rs592166	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs592622	0.93[YRI][hapmap]
rs593800	1.00[JPT][hapmap];0.88[YRI][hapmap];0.94[ASN][1000 genomes]
rs594122	0.81[ASN][1000 genomes]
rs595435	0.93[YRI][hapmap]
rs605652	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs607864	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs613315	0.93[YRI][hapmap]
rs617231	0.82[CHB][hapmap]
rs626013	0.94[ASN][1000 genomes]
rs626531	0.82[CHB][hapmap]
rs626700	0.93[YRI][hapmap]
rs631370	0.82[CHB][hapmap]
rs632351	0.85[ASN][1000 genomes]
rs641655	0.82[CHB][hapmap];0.86[YRI][hapmap]
rs641958	1.00[JPT][hapmap]
rs660274	1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[ASN][1000 genomes]
rs666735	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs679745	0.82[CHB][hapmap]
rs686009	0.88[YRI][hapmap]
rs7102107	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7118119	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7126522	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7948646	1.00[CEU][hapmap];0.80[YRI][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9634002	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9634003	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9634004	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9634018	1.00[CEU][hapmap];0.82[CHB][hapmap];0.80[YRI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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	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
3	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
4	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
5	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
6	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
7	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:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84787200-84789400	Enhancers	NHEK	skin
2	chr11:84788400-84792600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:84789200-84789600	Enhancers	Fetal Brain Male	brain
4	chr11:84789200-84789600	Bivalent Enhancer	HMEC	breast

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