Variant report

Variant	rs10452167
Chromosome Location	chr4:91323430-91323431
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10452166	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11930977	1.00[ASN][1000 genomes]
rs11931012	1.00[ASN][1000 genomes]
rs11931915	1.00[ASN][1000 genomes]
rs11931957	1.00[ASN][1000 genomes]
rs11934310	1.00[ASN][1000 genomes]
rs11937050	1.00[ASN][1000 genomes]
rs11938514	1.00[ASN][1000 genomes]
rs11947902	1.00[ASN][1000 genomes]
rs17017046	1.00[ASN][1000 genomes]
rs28433383	1.00[ASN][1000 genomes]
rs28450357	1.00[ASN][1000 genomes]
rs28455814	1.00[ASN][1000 genomes]
rs28516464	1.00[ASN][1000 genomes]
rs28631611	1.00[ASN][1000 genomes]
rs28631711	1.00[ASN][1000 genomes]
rs28669677	1.00[ASN][1000 genomes]
rs3971380	1.00[ASN][1000 genomes]
rs7660558	0.98[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7677243	1.00[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	nsv470053	chr4:90879613-91439573	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1007826	chr4:91049593-91438961	Enhancers Active TSS Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv537177	chr4:91049593-91438961	Bivalent/Poised TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv999065	chr4:91049593-91520073	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv1830936	chr4:91287204-91546380	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91296400-91325000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr4:91317800-91325400	Weak transcription	Pancreas	Pancrea
3	chr4:91321000-91327800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr4:91321400-91325400	Weak transcription	Fetal Stomach	stomach
5	chr4:91322200-91325000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:91323000-91325000	Weak transcription	Fetal Intestine Large	intestine

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