Variant report

Variant	rs9862867
Chromosome Location	chr3:161014327-161014328
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr3:161003253..161016100-chr3:161121496..161137189,33	MCF-7	breast:
4	chr3:161004827..161016513-chr3:161081728..161095319,56	MCF-7	breast:
5	chr3:161012665..161014668-chr3:161015887..161018774,3	MCF-7	breast:
6	chr3:161007555..161015806-chr3:161127103..161142651,19	MCF-7	breast:

Variant related genes	Relation type
ENSG00000196542	Chromatin interaction

Extended variants
information (count: 113 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:110)

rs_ID	r²[population]
rs1017799	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12486069	0.87[ASN][1000 genomes]
rs12486111	0.89[JPT][hapmap]
rs12486998	0.89[JPT][hapmap]
rs12487002	0.90[JPT][hapmap]
rs12488127	0.89[JPT][hapmap]
rs12489004	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12489125	0.87[ASN][1000 genomes]
rs12490149	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12494520	0.82[AMR][1000 genomes]
rs12494725	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12496235	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs13315320	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13319558	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13319771	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1450518	0.88[JPT][hapmap]
rs16831850	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs16831864	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs16831882	0.87[ASN][1000 genomes]
rs16831942	0.87[ASN][1000 genomes]
rs2306209	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs28451189	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28704960	0.87[ASN][1000 genomes]
rs28713364	0.91[AMR][1000 genomes]
rs4296611	0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4352387	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4468992	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs4580574	0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4635725	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs57903480	0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs59567999	0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs59757775	0.90[ASN][1000 genomes]
rs59776766	0.87[ASN][1000 genomes]
rs60121330	0.87[ASN][1000 genomes]
rs6441350	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6441363	0.88[AMR][1000 genomes]
rs6441365	0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6441372	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6441375	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs6762064	0.88[JPT][hapmap];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6774919	0.88[JPT][hapmap];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6775446	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6775931	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6778186	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6781086	0.85[AMR][1000 genomes]
rs6782415	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6782518	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6785714	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6787447	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6787697	0.80[AMR][1000 genomes]
rs6788738	0.91[AMR][1000 genomes]
rs6790805	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6793980	0.83[AMR][1000 genomes]
rs6794601	0.89[JPT][hapmap]
rs6796168	0.87[ASN][1000 genomes]
rs6800515	0.82[CHB][hapmap]
rs6801664	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6805976	0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs73017340	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73026933	0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73026967	0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73026968	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73026983	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73026987	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73026989	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73878309	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7615833	1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7615868	0.89[JPT][hapmap];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7624791	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7626773	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7634299	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7651924	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7652624	0.82[CHB][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9290070	0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9290071	0.94[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9810351	0.87[ASN][1000 genomes]
rs9812574	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9818470	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9818835	0.87[ASN][1000 genomes]
rs9818992	0.82[ASN][1000 genomes]
rs9819793	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9822705	1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9822916	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9823424	0.87[ASN][1000 genomes]
rs9824535	0.87[ASN][1000 genomes]
rs9824805	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9826857	0.87[ASN][1000 genomes]
rs9830183	0.91[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9833270	0.88[JPT][hapmap];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9834806	0.88[AMR][1000 genomes]
rs9835530	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9838945	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9841871	0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9842290	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9847842	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9850455	0.90[JPT][hapmap]
rs9851699	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9855112	0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9855572	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9856742	0.80[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9858907	0.87[ASN][1000 genomes]
rs9859641	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9860980	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9871753	0.88[JPT][hapmap];0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9872514	0.90[JPT][hapmap]
rs9876077	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9877309	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9880536	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9884100	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9985364	0.94[AMR][1000 genomes];0.97[ASN][1000 genomes]

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	chr3:160994600-161016800	Weak transcription	Right Ventricle	heart
2	chr3:161009800-161016600	Weak transcription	Pancreas	Pancrea
3	chr3:161010000-161015000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:161010400-161016600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr3:161014200-161014400	ZNF genes & repeats	HSMM	muscle

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