Variant report

Variant	rs9850455
Chromosome Location	chr3:161017192-161017193
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:161006300..161011924-chr3:161012842..161019057,8	MCF-7	breast:
2	chr3:161006306..161018540-chr3:161080036..161092321,36	MCF-7	breast:
3	chr3:161016824..161018347-chr3:161087834..161089442,2	MCF-7	breast:
4	chr3:161012665..161014668-chr3:161015887..161018774,3	MCF-7	breast:
5	chr3:161016261..161017784-chr3:161018167..161020383,2	MCF-7	breast:
6	chr3:161015254..161017853-chr3:161017997..161020969,3	MCF-7	breast:
7	chr3:161016283..161019052-chr3:161060342..161062317,2	MCF-7	breast:
8	chr3:161009005..161010540-chr3:161015594..161017754,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000196542	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:123)

rs_ID	r²[population]
rs1017799	0.90[JPT][hapmap]
rs10804790	0.96[EUR][1000 genomes]
rs1154701	0.86[CEU][hapmap];0.90[EUR][1000 genomes]
rs12486253	0.80[EUR][1000 genomes]
rs12487002	0.80[JPT][hapmap]
rs12490149	0.89[JPT][hapmap]
rs13083229	0.82[CEU][hapmap]
rs13319558	0.90[JPT][hapmap]
rs13319771	0.88[JPT][hapmap]
rs1382427	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1382428	0.96[EUR][1000 genomes]
rs1478565	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs1478568	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs1600209	0.96[EUR][1000 genomes]
rs163327	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs163328	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs189270	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs1993891	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2306209	0.89[JPT][hapmap]
rs2404340	0.98[EUR][1000 genomes]
rs28515190	0.96[EUR][1000 genomes]
rs336541	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs336543	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs336548	0.96[EUR][1000 genomes]
rs336567	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336569	0.93[EUR][1000 genomes]
rs336570	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336572	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs336577	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs336579	0.92[EUR][1000 genomes]
rs336580	0.96[CEU][hapmap]
rs336583	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336585	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336586	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs336589	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336590	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336591	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs336593	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs339101	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs3849524	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4273380	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs4290817	0.83[CEU][hapmap]
rs4350933	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4352387	0.89[JPT][hapmap]
rs4370045	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs4414866	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs4468992	0.90[JPT][hapmap]
rs4493448	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4493449	1.00[CEU][hapmap]
rs4518145	0.86[EUR][1000 genomes]
rs455386	0.82[EUR][1000 genomes]
rs456611	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs457272	0.91[EUR][1000 genomes]
rs459697	0.92[EUR][1000 genomes]
rs4597724	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs460165	0.88[EUR][1000 genomes]
rs460508	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs461638	0.82[EUR][1000 genomes]
rs462413	0.82[EUR][1000 genomes]
rs462514	0.85[CEU][hapmap]
rs463928	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs464766	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs465985	0.83[EUR][1000 genomes]
rs466399	0.88[EUR][1000 genomes]
rs4856714	0.83[CEU][hapmap]
rs4856739	0.89[EUR][1000 genomes]
rs4856767	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs4856768	0.81[EUR][1000 genomes]
rs62279921	0.91[EUR][1000 genomes]
rs6441370	0.90[EUR][1000 genomes]
rs6441371	0.88[EUR][1000 genomes]
rs6441373	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6441375	0.89[JPT][hapmap]
rs6762645	0.96[EUR][1000 genomes]
rs6765269	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs6774276	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs6775446	0.89[JPT][hapmap]
rs6775627	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6775931	0.89[JPT][hapmap]
rs6782415	0.89[JPT][hapmap]
rs6782518	0.89[JPT][hapmap]
rs6785714	0.84[JPT][hapmap]
rs6789388	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs6791213	0.82[CEU][hapmap]
rs6794601	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7611367	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs7613358	0.83[CEU][hapmap]
rs7615592	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs7623206	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs7626773	0.90[JPT][hapmap]
rs7627528	0.81[EUR][1000 genomes]
rs7629987	0.98[EUR][1000 genomes]
rs7631479	0.88[CEU][hapmap]
rs7632797	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs7633186	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs7634299	0.90[JPT][hapmap]
rs7638668	0.96[EUR][1000 genomes]
rs7647327	1.00[EUR][1000 genomes]
rs7651924	0.90[JPT][hapmap]
rs7652267	0.82[CEU][hapmap]
rs7653233	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7653361	1.00[CEU][hapmap];0.99[EUR][1000 genomes]
rs9290073	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9290074	0.96[EUR][1000 genomes]
rs975323	0.99[EUR][1000 genomes]
rs9790314	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9815222	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs9819793	0.86[JPT][hapmap]
rs9821201	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9822916	0.89[JPT][hapmap]
rs9824805	0.90[JPT][hapmap]
rs9835530	0.90[JPT][hapmap]
rs9839527	0.81[EUR][1000 genomes]
rs9846756	0.97[EUR][1000 genomes]
rs9847842	0.89[JPT][hapmap]
rs9859641	0.89[JPT][hapmap]
rs9860980	0.88[JPT][hapmap]
rs9862867	0.90[JPT][hapmap]
rs9863590	0.81[EUR][1000 genomes]
rs9870059	0.96[CEU][hapmap];1.00[EUR][1000 genomes]
rs9872514	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9877309	0.86[JPT][hapmap]
rs9880536	0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv1015063	chr3:160918307-161024070	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv829770	chr3:160989573-161069223	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161015000-161017600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:161016600-161017200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr3:161016600-161017200	ZNF genes & repeats	Pancreas	Pancrea
4	chr3:161017000-161021400	Weak transcription	Aorta	Aorta
5	chr3:161017000-161033000	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links