Variant report

Variant	rs479847
Chromosome Location	chr2:31803023-31803024
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	chr17:79477743..79480013-chr2:31802831..31804797,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000184009	Chromatin interaction
ENSG00000266077	Chromatin interaction

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10204002	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1090817	0.88[ASN][1000 genomes]
rs11124267	0.85[ASN][1000 genomes]
rs11883601	0.82[EUR][1000 genomes]
rs12691180	0.82[EUR][1000 genomes]
rs12712320	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12997020	0.81[EUR][1000 genomes]
rs12997024	0.81[EUR][1000 genomes]
rs12997994	0.83[EUR][1000 genomes]
rs13001512	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13006356	0.88[ASN][1000 genomes]
rs13006358	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13027103	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13395648	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13432696	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17817040	0.83[EUR][1000 genomes]
rs1884722	0.81[EUR][1000 genomes]
rs28383032	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs28383050	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34091236	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34124115	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34509832	0.82[EUR][1000 genomes]
rs34687527	0.84[ASN][1000 genomes]
rs34893975	0.82[EUR][1000 genomes]
rs35118236	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs35574090	0.83[EUR][1000 genomes]
rs35702549	0.82[EUR][1000 genomes]
rs3731586	0.82[EUR][1000 genomes]
rs3754838	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3819844	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4141419	0.83[ASN][1000 genomes]
rs4952227	0.88[ASN][1000 genomes]
rs519704	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57754448	0.82[ASN][1000 genomes]
rs7562326	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7563475	0.84[ASN][1000 genomes]
rs7567093	0.88[ASN][1000 genomes]
rs7589579	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7594951	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7599086	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs806587	0.85[ASN][1000 genomes]
rs806590	0.88[ASN][1000 genomes]
rs806591	0.81[ASN][1000 genomes]
rs9332975	0.82[EUR][1000 genomes]
rs9789452	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532648	chr2:31591498-32312698	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv456030	chr2:31598823-31820256	Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv456041	chr2:31598823-31820256	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv581269	chr2:31598823-31820256	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv998853	chr2:31601455-31858961	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1005565	chr2:31603134-31868877	Genic enhancers Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1007179	chr2:31616112-31835410	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1005032	chr2:31616112-31867450	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv1013891	chr2:31629179-31854283	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv535612	chr2:31629179-31854283	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1002988	chr2:31767131-31996924	Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31803000-31803800	Weak transcription	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links