Variant report

Variant	rs16851335
Chromosome Location	chr3:162398853-162398854
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10936308	0.87[ASN][1000 genomes]
rs11925750	0.83[ASN][1000 genomes]
rs11926645	0.86[ASN][1000 genomes]
rs12489679	0.87[ASN][1000 genomes]
rs12494243	0.82[ASN][1000 genomes]
rs12496614	0.80[ASN][1000 genomes]
rs12631404	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12632639	0.82[ASN][1000 genomes]
rs12635578	0.82[ASN][1000 genomes]
rs12635779	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12637998	0.82[ASN][1000 genomes]
rs13093719	0.86[ASN][1000 genomes]
rs1353556	0.80[ASN][1000 genomes]
rs1353557	0.80[ASN][1000 genomes]
rs2361609	0.82[ASN][1000 genomes]
rs4858911	0.81[ASN][1000 genomes]
rs55807361	0.86[ASN][1000 genomes]
rs56162745	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56815734	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57617609	0.82[ASN][1000 genomes]
rs58194889	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58604878	0.93[ASN][1000 genomes]
rs59027724	0.86[ASN][1000 genomes]
rs59268288	0.84[AFR][1000 genomes]
rs59307821	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61170375	0.82[ASN][1000 genomes]
rs62294573	0.83[ASN][1000 genomes]
rs62294581	0.80[ASN][1000 genomes]
rs6441546	0.81[ASN][1000 genomes]
rs66614152	0.95[ASN][1000 genomes]
rs6775650	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6808822	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73010393	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73010394	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73010402	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73876049	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876051	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876052	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876057	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876059	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876061	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876063	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876065	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73876066	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73876068	0.82[ASN][1000 genomes]
rs73876069	0.82[ASN][1000 genomes]
rs73876071	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73876072	0.82[ASN][1000 genomes]
rs73876101	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7426713	0.81[ASN][1000 genomes]
rs7633892	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7640151	0.83[ASN][1000 genomes]
rs7652225	0.93[ASN][1000 genomes]
rs7652373	0.87[ASN][1000 genomes]
rs9839936	0.87[ASN][1000 genomes]
rs9844124	0.87[ASN][1000 genomes]
rs9867696	0.80[ASN][1000 genomes]
rs9874108	0.86[ASN][1000 genomes]
rs9883543	0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006802	chr3:161921063-162599175	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv428424	chr3:162145988-163033943	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1012160	chr3:162182166-162540478	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv592201	chr3:162188625-163142162	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv829775	chr3:162211618-162406402	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv470994	chr3:162217993-162945834	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1005142	chr3:162284967-162447818	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv877758	chr3:162287573-162521339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv877759	chr3:162303276-162521339	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv877761	chr3:162346392-162521339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv592208	chr3:162369863-162437102	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv460957	chr3:162370941-162399269	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
13	nsv592209	chr3:162370941-162399269	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
14	nsv1005637	chr3:162379324-162635451	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162395400-162399000	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr3:162395600-162399000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr3:162398000-162399000	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links