Variant report

Variant	rs10176630
Chromosome Location	chr2:134273902-134273903
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	chr2:134265911..134268884-chr2:134269496..134274997,4	MCF-7	breast:

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10172908	1.00[EUR][1000 genomes]
rs10179509	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10180776	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10182352	1.00[YRI][hapmap];1.00[EUR][1000 genomes]
rs10204302	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11904353	1.00[EUR][1000 genomes]
rs13383175	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13383603	1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13396221	1.00[EUR][1000 genomes]
rs13399787	0.82[YRI][hapmap]
rs13402934	0.93[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13406195	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13406470	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs13410388	1.00[EUR][1000 genomes]
rs13419194	0.82[YRI][hapmap];1.00[EUR][1000 genomes]
rs13432659	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16825509	0.89[YRI][hapmap]
rs1897430	0.90[YRI][hapmap];1.00[EUR][1000 genomes]
rs1897431	1.00[EUR][1000 genomes]
rs28420171	1.00[EUR][1000 genomes]
rs28634361	1.00[EUR][1000 genomes]
rs6718180	1.00[EUR][1000 genomes]
rs6727895	1.00[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	nsv997821	chr2:133868822-134360220	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535927	chr2:133868822-134360220	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1002488	chr2:133890159-134275312	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv535928	chr2:133890159-134275312	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv1003624	chr2:134126928-134583203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	esv2830192	chr2:134259612-134311713	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv1006101	chr2:134263288-134973917	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 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	chr2:134267000-134275200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:134268200-134290000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:134269000-134276000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:134269000-134276600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:134270600-134275600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:134271600-134274000	Enhancers	Fetal Brain Male	brain
7	chr2:134272400-134274000	Enhancers	Brain Hippocampus Middle	brain
8	chr2:134272600-134275800	Enhancers	Brain Substantia Nigra	brain
9	chr2:134273000-134274000	Enhancers	Brain Angular Gyrus	brain
10	chr2:134273000-134274000	Enhancers	Brain Anterior Caudate	brain
11	chr2:134273800-134274200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:134273800-134274800	Enhancers	Liver	Liver
13	chr2:134273800-134274800	Enhancers	Fetal Brain Female	brain
14	chr2:134273800-134275200	Enhancers	NHDF-Ad	bronchial

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